Linked Data
ClinVar Variation Id:
1505069
ClinVar RCV Id:
RCV002047961
dbSNP Id:
rs2152875227
gnomAD v4:
2-71611491-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71611491G>C , CM000664.2:g.71611491G>C | GRCh38 |
| NC_000002.11:g.71838621G>C , CM000664.1:g.71838621G>C | GRCh37 |
| NC_000002.10:g.71692129G>C | NCBI36 |
| NG_008694.1:g.162869G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698057.1:c.1500G>C | ENSP00000513536.1:p.Met500Ile | |
| ENST00000698058.1:c.717G>C | ENSP00000513537.1:p.Met239Ile | |
| ENST00000698059.1:c.675G>C | ENSP00000513538.1:p.Met225Ile | |
| ENST00000258104.8:c.4032G>C MANE Plus Clinical | ENSP00000258104.3:p.Met1344Ile | |
| ENST00000410020.8:c.4086G>C MANE Select | ENSP00000386881.3:p.Met1362Ile | |
| ENST00000258104.7:c.4032G>C | ENSP00000258104.3:p.Met1344Ile | |
| ENST00000394120.6:c.4035G>C | ENSP00000377678.2:p.Met1345Ile | |
| ENST00000409366.5:c.4035G>C | ENSP00000386512.1:p.Met1345Ile | |
| ENST00000409582.7:c.4083G>C | ENSP00000386547.3:p.Met1361Ile | |
| ENST00000409651.5:c.4128G>C | ENSP00000386683.1:p.Met1376Ile | |
| ENST00000409744.5:c.3993G>C | ENSP00000386285.1:p.Met1331Ile | |
| ENST00000409762.5:c.4083G>C | ENSP00000387137.1:p.Met1361Ile | |
| ENST00000410020.7:c.4086G>C | ENSP00000386881.3:p.Met1362Ile | |
| ENST00000410041.1:c.4086G>C | ENSP00000386617.1:p.Met1362Ile | |
| ENST00000413539.6:c.4125G>C | ENSP00000407046.2:p.Met1375Ile | |
| ENST00000429174.6:c.4032G>C | ENSP00000398305.2:p.Met1344Ile | |
| ENST00000468173.1:n.268G>C | ||
| ENST00000472873.5:n.416G>C | ||
| ENST00000479049.6:n.917G>C | ||
| ENST00000487180.5:n.251G>C | ||
| ENST00000494501.5:n.366-36G>C | ||
| NM_001130455.1:c.4035G>C | NP_001123927.1:p.Met1345Ile | |
| NM_001130976.1:c.3990G>C | NP_001124448.1:p.Met1330Ile | |
| NM_001130977.1:c.3990G>C | NP_001124449.1:p.Met1330Ile | |
| NM_001130978.1:c.4032G>C | NP_001124450.1:p.Met1344Ile | |
| NM_001130979.1:c.4125G>C | NP_001124451.1:p.Met1375Ile | |
| NM_001130980.1:c.4083G>C | NP_001124452.1:p.Met1361Ile | |
| NM_001130981.1:c.4083G>C | NP_001124453.1:p.Met1361Ile | |
| NM_001130982.1:c.4128G>C | NP_001124454.1:p.Met1376Ile | |
| NM_001130983.1:c.4035G>C | NP_001124455.1:p.Met1345Ile | |
| NM_001130984.1:c.3993G>C | NP_001124456.1:p.Met1331Ile | |
| NM_001130985.1:c.4086G>C | NP_001124457.1:p.Met1362Ile | |
| NM_001130986.1:c.3993G>C | NP_001124458.1:p.Met1331Ile | |
| NM_001130987.1:c.4086G>C | NP_001124459.1:p.Met1362Ile | |
| NM_003494.3:c.4032G>C | NP_003485.1:p.Met1344Ile | |
| XM_005264584.3:c.4128G>C | XP_005264641.1:p.Met1376Ile | |
| XM_005264585.3:c.4125G>C | XP_005264642.1:p.Met1375Ile | |
| XM_005264584.4:c.4128G>C | XP_005264641.1:p.Met1376Ile | |
| XM_005264585.5:c.4125G>C | XP_005264642.1:p.Met1375Ile | |
| XR_001738969.1:n.4286G>C | ||
| NM_001130987.2:c.4086G>C MANE Select | NP_001124459.1:p.Met1362Ile | |
| NM_001130455.2:c.4035G>C | NP_001123927.1:p.Met1345Ile | |
| NM_001130976.2:c.3990G>C | NP_001124448.1:p.Met1330Ile | |
| NM_001130977.2:c.3990G>C | NP_001124449.1:p.Met1330Ile | |
| NM_001130978.2:c.4032G>C | NP_001124450.1:p.Met1344Ile | |
| NM_001130979.2:c.4125G>C | NP_001124451.1:p.Met1375Ile | |
| NM_001130980.2:c.4083G>C | NP_001124452.1:p.Met1361Ile | |
| NM_001130981.2:c.4083G>C | NP_001124453.1:p.Met1361Ile | |
| NM_001130982.2:c.4128G>C | NP_001124454.1:p.Met1376Ile | |
| NM_001130983.2:c.4035G>C | NP_001124455.1:p.Met1345Ile | |
| NM_001130984.2:c.3993G>C | NP_001124456.1:p.Met1331Ile | |
| NM_001130985.2:c.4086G>C | NP_001124457.1:p.Met1362Ile | |
| NM_001130986.2:c.3993G>C | NP_001124458.1:p.Met1331Ile | |
| NM_003494.4:c.4032G>C MANE Plus Clinical | NP_003485.1:p.Met1344Ile |