Linked Data
dbSNP Id:
rs1306661080
gnomAD v4:
1-149927960-G-A
MyVariant Identifiers:
chr1:g.149927960G>A (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149927960G>A , CM000663.2:g.149927960G>A | GRCh38 |
| NC_000001.10:g.149899852G>A , CM000663.1:g.149899852G>A | GRCh37 |
| NC_000001.9:g.148166476G>A | NCBI36 |
| NG_032777.1:g.5293C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.8:c.-201C>T | ENSP00000271628.8:n.-201C>T | |
| NM_005850.4:c.-201C>T | NP_005841.1:n.-201C>T |