Linked Data
gnomAD v4:
8-63039032-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.63039032C>T , CM000670.2:g.63039032C>T | GRCh38 |
| NC_000008.10:g.63951591C>T , CM000670.1:g.63951591C>T | GRCh37 |
| NC_000008.9:g.64114145C>T | NCBI36 |
| NG_028126.1:g.5020G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000677327.1:n.376G>A | ||
| ENST00000679326.1:c.-264G>A | ENSP00000504262.1:n.-264G>A | |
| ENST00000260118.6:c.-264G>A | ENSP00000260118.6:n.-264G>A | |
| NM_003878.2:c.-264G>A | NP_003869.1:n.-264G>A | |
| XM_011517623.1:c.-264G>A | XP_011515925.1:n.-264G>A |