Linked Data
dbSNP Id:
rs760481746
ExAC:
5:178421889 C / A
gnomAD v2:
5-178421889-C-A
gnomAD v3:
5-178994888-C-A
gnomAD v4:
5-178994888-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.178994888C>A , CM000667.2:g.178994888C>A | GRCh38 |
| NC_000005.9:g.178421889C>A , CM000667.1:g.178421889C>A | GRCh37 |
| NC_000005.8:g.178354495C>A | NCBI36 |
| NG_008105.1:g.5236G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000517717.3:c.57G>T MANE Select | ENSP00000430767.1:p.Ala19= | |
| ENST00000650031.1:c.57G>T | ENSP00000497110.1:p.Ala19= | |
| ENST00000231188.9:c.57G>T | ENSP00000231188.5:p.Ala19= | |
| ENST00000517717.1:c.57G>T | ENSP00000430767.1:p.Ala19= | |
| NM_000843.3:c.57G>T | NP_000834.2:p.Ala19= | |
| NM_000843.4:c.57G>T MANE Select | NP_000834.2:p.Ala19= |