Linked Data
gnomAD v4:
8-63039059-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.63039059C>A , CM000670.2:g.63039059C>A | GRCh38 |
| NC_000008.10:g.63951618C>A , CM000670.1:g.63951618C>A | GRCh37 |
| NC_000008.9:g.64114172C>A | NCBI36 |
| NG_028126.1:g.4993G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000677327.1:n.349G>T | ||
| ENST00000679326.1:c.-291G>T | ENSP00000504262.1:n.-291G>T | |
| ENST00000260118.6:c.-291G>T | ENSP00000260118.6:n.-291G>T | |
| XM_011517623.1:c.-291G>T | XP_011515925.1:n.-291G>T |