Linked Data
ClinVar Variation Id:
336972
dbSNP Id:
rs369949055
ExAC:
2:71840547 T / C
gnomAD v2:
2-71840547-T-C
gnomAD v3:
2-71613417-T-C
gnomAD v4:
2-71613417-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71613417T>C , CM000664.2:g.71613417T>C | GRCh38 |
| NC_000002.11:g.71840547T>C , CM000664.1:g.71840547T>C | GRCh37 |
| NC_000002.10:g.71694055T>C | NCBI36 |
| NG_008694.1:g.164795T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698057.1:c.1878+7T>C | ENSP00000513536.1:n.1878+7T>C | |
| ENST00000698058.1:c.1095+7T>C | ENSP00000513537.1:n.1095+7T>C | |
| ENST00000698059.1:c.1053+7T>C | ENSP00000513538.1:n.1053+7T>C | |
| ENST00000258104.8:c.4410+7T>C MANE Plus Clinical | ENSP00000258104.3:n.4410+7T>C | |
| ENST00000410020.8:c.4464+7T>C MANE Select | ENSP00000386881.3:n.4464+7T>C | |
| ENST00000258104.7:c.4410+7T>C | ENSP00000258104.3:n.4410+7T>C | |
| ENST00000394120.6:c.4413+7T>C | ENSP00000377678.2:n.4413+7T>C | |
| ENST00000409366.5:c.4413+7T>C | ENSP00000386512.1:n.4413+7T>C | |
| ENST00000409582.7:c.4461+7T>C | ENSP00000386547.3:n.4461+7T>C | |
| ENST00000409651.5:c.4506+7T>C | ENSP00000386683.1:n.4506+7T>C | |
| ENST00000409744.5:c.4371+7T>C | ENSP00000386285.1:n.4371+7T>C | |
| ENST00000409762.5:c.4461+7T>C | ENSP00000387137.1:n.4461+7T>C | |
| ENST00000410020.7:c.4464+7T>C | ENSP00000386881.3:n.4464+7T>C | |
| ENST00000410041.1:c.4464+7T>C | ENSP00000386617.1:n.4464+7T>C | |
| ENST00000413539.6:c.4503+7T>C | ENSP00000407046.2:n.4503+7T>C | |
| ENST00000429174.6:c.4410+7T>C | ENSP00000398305.2:n.4410+7T>C | |
| ENST00000468173.1:n.646+7T>C | ||
| ENST00000479049.6:n.1295+7T>C | ||
| NM_001130455.1:c.4413+7T>C | NP_001123927.1:n.4413+7T>C | |
| NM_001130976.1:c.4368+7T>C | NP_001124448.1:n.4368+7T>C | |
| NM_001130977.1:c.4368+7T>C | NP_001124449.1:n.4368+7T>C | |
| NM_001130978.1:c.4410+7T>C | NP_001124450.1:n.4410+7T>C | |
| NM_001130979.1:c.4503+7T>C | NP_001124451.1:n.4503+7T>C | |
| NM_001130980.1:c.4461+7T>C | NP_001124452.1:n.4461+7T>C | |
| NM_001130981.1:c.4461+7T>C | NP_001124453.1:n.4461+7T>C | |
| NM_001130982.1:c.4506+7T>C | NP_001124454.1:n.4506+7T>C | |
| NM_001130983.1:c.4413+7T>C | NP_001124455.1:n.4413+7T>C | |
| NM_001130984.1:c.4371+7T>C | NP_001124456.1:n.4371+7T>C | |
| NM_001130985.1:c.4464+7T>C | NP_001124457.1:n.4464+7T>C | |
| NM_001130986.1:c.4371+7T>C | NP_001124458.1:n.4371+7T>C | |
| NM_001130987.1:c.4464+7T>C | NP_001124459.1:n.4464+7T>C | |
| NM_003494.3:c.4410+7T>C | NP_003485.1:n.4410+7T>C | |
| XM_005264584.3:c.4506+7T>C | XP_005264641.1:n.4506+7T>C | |
| XM_005264585.3:c.4503+7T>C | XP_005264642.1:n.4503+7T>C | |
| XM_005264584.4:c.4506+7T>C | XP_005264641.1:n.4506+7T>C | |
| XM_005264585.5:c.4503+7T>C | XP_005264642.1:n.4503+7T>C | |
| XR_001738969.1:n.4664+7T>C | ||
| NM_001130987.2:c.4464+7T>C MANE Select | NP_001124459.1:n.4464+7T>C | |
| NM_001130455.2:c.4413+7T>C | NP_001123927.1:n.4413+7T>C | |
| NM_001130976.2:c.4368+7T>C | NP_001124448.1:n.4368+7T>C | |
| NM_001130977.2:c.4368+7T>C | NP_001124449.1:n.4368+7T>C | |
| NM_001130978.2:c.4410+7T>C | NP_001124450.1:n.4410+7T>C | |
| NM_001130979.2:c.4503+7T>C | NP_001124451.1:n.4503+7T>C | |
| NM_001130980.2:c.4461+7T>C | NP_001124452.1:n.4461+7T>C | |
| NM_001130981.2:c.4461+7T>C | NP_001124453.1:n.4461+7T>C | |
| NM_001130982.2:c.4506+7T>C | NP_001124454.1:n.4506+7T>C | |
| NM_001130983.2:c.4413+7T>C | NP_001124455.1:n.4413+7T>C | |
| NM_001130984.2:c.4371+7T>C | NP_001124456.1:n.4371+7T>C | |
| NM_001130985.2:c.4464+7T>C | NP_001124457.1:n.4464+7T>C | |
| NM_001130986.2:c.4371+7T>C | NP_001124458.1:n.4371+7T>C | |
| NM_003494.4:c.4410+7T>C MANE Plus Clinical | NP_003485.1:n.4410+7T>C |