Linked Data
ClinVar Variation Id:
1602051
ClinVar RCV Id:
RCV002127698
dbSNP Id:
rs769798393
ExAC:
4:103681929 G / T
gnomAD v2:
4-103681929-G-T
gnomAD v4:
4-102760772-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.102760772G>T , CM000666.2:g.102760772G>T | GRCh38 |
| NC_000004.11:g.103681929G>T , CM000666.1:g.103681929G>T | GRCh37 |
| NC_000004.10:g.103900974G>T | NCBI36 |
| NG_012804.1:g.5223C>A | |
| NG_012804.2:g.5223C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000642252.1:c.123C>A | ENSP00000495483.1:p.Pro41= | |
| ENST00000644159.1:c.123C>A | ENSP00000494462.1:p.Pro41= | |
| ENST00000644545.1:c.123C>A | ENSP00000493992.1:p.Pro41= | |
| ENST00000644965.1:c.123C>A | ENSP00000495818.1:p.Pro41= | |
| ENST00000645348.1:c.123C>A | ENSP00000495363.1:p.Pro41= | |
| ENST00000646311.1:c.123C>A | ENSP00000493465.1:p.Pro41= | |
| ENST00000646727.1:c.123C>A | ENSP00000493519.1:p.Pro41= | |
| ENST00000647097.2:c.123C>A MANE Select | ENSP00000495247.1:p.Pro41= | |
| ENST00000226578.8:c.123C>A | ENSP00000226578.4:p.Pro41= | |
| ENST00000505239.1:c.123C>A | ENSP00000427322.1:p.Pro41= | |
| ENST00000507358.1:n.223C>A | ||
| ENST00000511813.1:c.123C>A | ENSP00000422001.1:p.Pro41= | |
| ENST00000514430.5:n.170C>A | ||
| NM_005908.3:c.123C>A | NP_005899.3:p.Pro41= | |
| XM_017008203.1:c.-414C>A | XP_016863692.1:n.-414C>A | |
| XM_017008204.2:c.-402C>A | XP_016863693.1:n.-402C>A | |
| NM_005908.4:c.123C>A MANE Select | NP_005899.3:p.Pro41= |