Linked Data
dbSNP Id:
rs149199162
ExAC:
5:148206776 G / T
gnomAD v2:
5-148206776-G-T
gnomAD v3:
5-148827213-G-T
gnomAD v4:
5-148827213-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.148827213G>T , CM000667.2:g.148827213G>T | GRCh38 |
| NC_000005.9:g.148206776G>T , CM000667.1:g.148206776G>T | GRCh37 |
| NC_000005.8:g.148186969G>T | NCBI36 |
| NG_016421.1:g.5621G>T | |
| NG_016421.2:g.5621G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305988.6:c.382G>T MANE Select | ENSP00000305372.4:p.Ala128Ser | |
| ENST00000305988.5:c.382G>T | ENSP00000305372.4:p.Ala128Ser | |
| NM_000024.5:c.382G>T | NP_000015.1:p.Ala128Ser | |
| NM_000024.6:c.382G>T MANE Select | NP_000015.2:p.Ala128Ser |