Linked Data
gnomAD v4:
5-150155872-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.150155872T>G , CM000667.2:g.150155872T>G | GRCh38 |
| NC_000005.9:g.149535435T>G , CM000667.1:g.149535435T>G | GRCh37 |
| NC_000005.8:g.149515628T>G | NCBI36 |
| NG_023367.1:g.4988A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000523456.1:n.1A>C | ||
| XM_005268464.2:c.-628A>C | XP_005268521.1:n.-628A>C | |
| XM_011537659.1:c.-949A>C | XP_011535961.1:n.-949A>C |