Linked Data
gnomAD v4:
1-149927949-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.149927949C>G , CM000663.2:g.149927949C>G | GRCh38 |
| NC_000001.10:g.149899841C>G , CM000663.1:g.149899841C>G | GRCh37 |
| NC_000001.9:g.148166465C>G | NCBI36 |
| NG_032777.1:g.5304G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000271628.8:c.-190G>C | ENSP00000271628.8:n.-190G>C | |
| NM_005850.4:c.-190G>C | NP_005841.1:n.-190G>C |