Linked Data
ClinVar Variation Id:
264532
dbSNP Id:
rs138665246
ExAC:
5:127666299 G / A
gnomAD v2:
5-127666299-G-A
gnomAD v3:
5-128330607-G-A
gnomAD v4:
5-128330607-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128330607G>A , CM000667.2:g.128330607G>A | GRCh38 |
| NC_000005.9:g.127666299G>A , CM000667.1:g.127666299G>A | GRCh37 |
| NC_000005.8:g.127694198G>A | NCBI36 |
| NG_008750.1:g.212437C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000703783.1:n.1095C>T | ||
| ENST00000703785.1:n.1176C>T | ||
| ENST00000262464.9:c.4311C>T MANE Select | ENSP00000262464.4:p.Ser1437= | |
| ENST00000262464.8:c.4311C>T | ENSP00000262464.4:p.Ser1437= | |
| ENST00000507835.5:c.861C>T | ENSP00000426839.1:p.Ser287= | |
| ENST00000508053.5:c.4311C>T | ENSP00000424571.1:p.Ser1437= | |
| ENST00000508989.5:c.4212C>T | ENSP00000425596.1:p.Ser1404= | |
| ENST00000619499.4:c.4308C>T | ENSP00000482132.1:p.Ser1436= | |
| NM_001999.3:c.4311C>T | NP_001990.2:p.Ser1437= | |
| XM_017009228.2:c.4158C>T | XP_016864717.1:p.Ser1386= | |
| NM_001999.4:c.4311C>T MANE Select | NP_001990.2:p.Ser1437= |