Linked Data
dbSNP Id:
rs150422225
ExAC:
4:68619905 G / A
gnomAD v2:
4-68619905-G-A
gnomAD v3:
4-67754187-G-A
gnomAD v4:
4-67754187-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67754187G>A , CM000666.2:g.67754187G>A | GRCh38 |
| NC_000004.11:g.68619905G>A , CM000666.1:g.68619905G>A | GRCh37 |
| NC_000004.10:g.68302500G>A | NCBI36 |
| NG_009293.1:g.6900C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000226413.5:c.149C>T MANE Select | ENSP00000226413.5:p.Ala50Val | |
| ENST00000226413.4:c.149C>T | ENSP00000226413.4:p.Ala50Val | |
| ENST00000420975.2:c.149C>T | ENSP00000397561.2:p.Ala50Val | |
| NM_000406.2:c.149C>T | NP_000397.1:p.Ala50Val | |
| NM_001012763.1:c.149C>T | NP_001012781.1:p.Ala50Val | |
| NM_000406.3:c.149C>T MANE Select | NP_000397.1:p.Ala50Val | |
| NM_001012763.2:c.149C>T | NP_001012781.1:p.Ala50Val |