Linked Data
dbSNP Id:
rs1475861695
gnomAD v2:
1-149900225-T-A
gnomAD v3:
1-149928333-T-A
gnomAD v4:
1-149928333-T-A
MyVariant Identifiers:
chr1:g.149928333T>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149928333T>A , CM000663.2:g.149928333T>A | GRCh38 |
| NC_000001.10:g.149900225T>A , CM000663.1:g.149900225T>A | GRCh37 |
| NC_000001.9:g.148166849T>A | NCBI36 |
| NG_032777.1:g.4920A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.8:c.-574A>T | ENSP00000271628.8:n.-574A>T |