Linked Data
gnomAD v4:
X-106033459-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.106033459T>G , CM000685.2:g.106033459T>G | GRCh38 |
| NC_000023.10:g.105277450T>G , CM000685.1:g.105277450T>G | GRCh37 |
| NC_000023.9:g.105164106T>G | NCBI36 |
| NG_021252.1:g.10269A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372563.2:c.*41A>C MANE Select | ENSP00000361644.1:n.*41A>C | |
| ENST00000327674.8:c.*41A>C | ENSP00000329374.4:n.*41A>C | |
| ENST00000372563.1:c.*41A>C | ENSP00000361644.1:n.*41A>C | |
| NM_000354.5:c.*41A>C | NP_000345.2:n.*41A>C | |
| XM_006724683.1:c.*41A>C | XP_006724746.1:n.*41A>C | |
| XM_005262180.4:c.*234A>C | XP_005262237.1:n.*234A>C | |
| XM_006724683.2:c.*41A>C | XP_006724746.1:n.*41A>C | |
| NM_000354.6:c.*41A>C MANE Select | NP_000345.2:n.*41A>C |