Linked Data
gnomAD v4:
8-63039019-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.63039019C>A , CM000670.2:g.63039019C>A | GRCh38 |
| NC_000008.10:g.63951578C>A , CM000670.1:g.63951578C>A | GRCh37 |
| NC_000008.9:g.64114132C>A | NCBI36 |
| NG_028126.1:g.5033G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000677327.1:n.389G>T | ||
| ENST00000679326.1:c.-251G>T | ENSP00000504262.1:n.-251G>T | |
| ENST00000260118.6:c.-251G>T | ENSP00000260118.6:n.-251G>T | |
| NM_003878.2:c.-251G>T | NP_003869.1:n.-251G>T | |
| XM_011517623.1:c.-251G>T | XP_011515925.1:n.-251G>T |