Linked Data
gnomAD v4:
8-63039096-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.63039096T>C , CM000670.2:g.63039096T>C | GRCh38 |
| NC_000008.10:g.63951655T>C , CM000670.1:g.63951655T>C | GRCh37 |
| NC_000008.9:g.64114209T>C | NCBI36 |
| NG_028126.1:g.4956A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000677327.1:n.312A>G | ||
| ENST00000679326.1:c.-328A>G | ENSP00000504262.1:n.-328A>G | |
| ENST00000260118.6:c.-328A>G | ENSP00000260118.6:n.-328A>G | |
| XM_011517623.1:c.-328A>G | XP_011515925.1:n.-328A>G |