Linked Data
ClinVar Variation Id:
498983
dbSNP Id:
rs149979662
ExAC:
2:71795304 T / C
gnomAD v2:
2-71795304-T-C
gnomAD v3:
2-71568174-T-C
gnomAD v4:
2-71568174-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71568174T>C , CM000664.2:g.71568174T>C | GRCh38 |
| NC_000002.11:g.71795304T>C , CM000664.1:g.71795304T>C | GRCh37 |
| NC_000002.10:g.71648812T>C | NCBI36 |
| NG_008694.1:g.119552T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698057.1:c.72T>C | ENSP00000513536.1:p.Tyr24= | |
| ENST00000258104.8:c.2646T>C MANE Plus Clinical | ENSP00000258104.3:p.Tyr882= | |
| ENST00000410020.8:c.2700T>C MANE Select | ENSP00000386881.3:p.Tyr900= | |
| ENST00000258104.7:c.2646T>C | ENSP00000258104.3:p.Tyr882= | |
| ENST00000394120.6:c.2649T>C | ENSP00000377678.2:p.Tyr883= | |
| ENST00000409366.5:c.2649T>C | ENSP00000386512.1:p.Tyr883= | |
| ENST00000409582.7:c.2697T>C | ENSP00000386547.3:p.Tyr899= | |
| ENST00000409651.5:c.2742T>C | ENSP00000386683.1:p.Tyr914= | |
| ENST00000409744.5:c.2607T>C | ENSP00000386285.1:p.Tyr869= | |
| ENST00000409762.5:c.2697T>C | ENSP00000387137.1:p.Tyr899= | |
| ENST00000410020.7:c.2700T>C | ENSP00000386881.3:p.Tyr900= | |
| ENST00000410041.1:c.2700T>C | ENSP00000386617.1:p.Tyr900= | |
| ENST00000413539.6:c.2739T>C | ENSP00000407046.2:p.Tyr913= | |
| ENST00000429174.6:c.2646T>C | ENSP00000398305.2:p.Tyr882= | |
| NM_001130455.1:c.2649T>C | NP_001123927.1:p.Tyr883= | |
| NM_001130976.1:c.2604T>C | NP_001124448.1:p.Tyr868= | |
| NM_001130977.1:c.2604T>C | NP_001124449.1:p.Tyr868= | |
| NM_001130978.1:c.2646T>C | NP_001124450.1:p.Tyr882= | |
| NM_001130979.1:c.2739T>C | NP_001124451.1:p.Tyr913= | |
| NM_001130980.1:c.2697T>C | NP_001124452.1:p.Tyr899= | |
| NM_001130981.1:c.2697T>C | NP_001124453.1:p.Tyr899= | |
| NM_001130982.1:c.2742T>C | NP_001124454.1:p.Tyr914= | |
| NM_001130983.1:c.2649T>C | NP_001124455.1:p.Tyr883= | |
| NM_001130984.1:c.2607T>C | NP_001124456.1:p.Tyr869= | |
| NM_001130985.1:c.2700T>C | NP_001124457.1:p.Tyr900= | |
| NM_001130986.1:c.2607T>C | NP_001124458.1:p.Tyr869= | |
| NM_001130987.1:c.2700T>C | NP_001124459.1:p.Tyr900= | |
| NM_003494.3:c.2646T>C | NP_003485.1:p.Tyr882= | |
| XM_005264584.3:c.2742T>C | XP_005264641.1:p.Tyr914= | |
| XM_005264585.3:c.2739T>C | XP_005264642.1:p.Tyr913= | |
| XM_005264584.4:c.2742T>C | XP_005264641.1:p.Tyr914= | |
| XM_005264585.5:c.2739T>C | XP_005264642.1:p.Tyr913= | |
| XR_001738969.1:n.2900T>C | ||
| NM_001130987.2:c.2700T>C MANE Select | NP_001124459.1:p.Tyr900= | |
| NM_001130455.2:c.2649T>C | NP_001123927.1:p.Tyr883= | |
| NM_001130976.2:c.2604T>C | NP_001124448.1:p.Tyr868= | |
| NM_001130977.2:c.2604T>C | NP_001124449.1:p.Tyr868= | |
| NM_001130978.2:c.2646T>C | NP_001124450.1:p.Tyr882= | |
| NM_001130979.2:c.2739T>C | NP_001124451.1:p.Tyr913= | |
| NM_001130980.2:c.2697T>C | NP_001124452.1:p.Tyr899= | |
| NM_001130981.2:c.2697T>C | NP_001124453.1:p.Tyr899= | |
| NM_001130982.2:c.2742T>C | NP_001124454.1:p.Tyr914= | |
| NM_001130983.2:c.2649T>C | NP_001124455.1:p.Tyr883= | |
| NM_001130984.2:c.2607T>C | NP_001124456.1:p.Tyr869= | |
| NM_001130985.2:c.2700T>C | NP_001124457.1:p.Tyr900= | |
| NM_001130986.2:c.2607T>C | NP_001124458.1:p.Tyr869= | |
| NM_003494.4:c.2646T>C MANE Plus Clinical | NP_003485.1:p.Tyr882= |