Linked Data
dbSNP Id:
rs965282668
gnomAD v3:
1-149927952-C-G
gnomAD v4:
1-149927952-C-G
MyVariant Identifiers:
chr1:g.149927952C>G (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149927952C>G , CM000663.2:g.149927952C>G | GRCh38 |
| NC_000001.10:g.149899844C>G , CM000663.1:g.149899844C>G | GRCh37 |
| NC_000001.9:g.148166468C>G | NCBI36 |
| NG_032777.1:g.5301G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.8:c.-193G>C | ENSP00000271628.8:n.-193G>C | |
| NM_005850.4:c.-193G>C | NP_005841.1:n.-193G>C |