Linked Data
gnomAD v4:
17-63832083-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63832083A>G , CM000679.2:g.63832083A>G | GRCh38 |
| NC_000017.10:g.61909443A>G , CM000679.1:g.61909443A>G | GRCh37 |
| NC_000017.9:g.59263175A>G | NCBI36 |
| NG_053004.1:g.15909T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000448276.7:c.*855T>C MANE Select | ENSP00000392617.2:n.*855T>C | |
| ENST00000613943.4:c.2340T>C | ENSP00000483605.1:n.2340T>C | |
| NM_001098426.1:c.*855T>C | NP_001091896.1:n.*855T>C | |
| XM_005257604.2:c.*855T>C | XP_005257661.2:n.*855T>C | |
| NM_001330439.1:c.*855T>C | NP_001317368.1:n.*855T>C | |
| NM_001330440.1:c.*855T>C | NP_001317369.1:n.*855T>C | |
| NM_001098426.2:c.*855T>C MANE Select | NP_001091896.1:n.*855T>C | |
| NM_001330440.2:c.*855T>C | NP_001317369.1:n.*855T>C |