Linked Data
gnomAD v4:
6-136822469-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.136822469T>A , CM000668.2:g.136822469T>A | GRCh38 |
| NC_000006.11:g.137143607T>A , CM000668.1:g.137143607T>A | GRCh37 |
| NC_000006.10:g.137185300T>A | NCBI36 |
| NG_008462.1:g.4890T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_006715502.1:c.-197T>A | XP_006715565.1:n.-197T>A | |
| XM_011535900.1:c.-197T>A | XP_011534202.1:n.-197T>A | |
| XM_006715502.2:c.-197T>A | XP_006715565.1:n.-197T>A | |
| XM_017010934.2:c.-197T>A | XP_016866423.1:n.-197T>A |