Linked Data
gnomAD v4:
8-63039091-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.63039091T>G , CM000670.2:g.63039091T>G | GRCh38 |
| NC_000008.10:g.63951650T>G , CM000670.1:g.63951650T>G | GRCh37 |
| NC_000008.9:g.64114204T>G | NCBI36 |
| NG_028126.1:g.4961A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000677327.1:n.317A>C | ||
| ENST00000679326.1:c.-323A>C | ENSP00000504262.1:n.-323A>C | |
| ENST00000260118.6:c.-323A>C | ENSP00000260118.6:n.-323A>C | |
| XM_011517623.1:c.-323A>C | XP_011515925.1:n.-323A>C |