Linked Data
gnomAD v4:
2-149569835-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.149569835C>T , CM000664.2:g.149569835C>T | GRCh38 |
| NC_000002.11:g.150426349C>T , CM000664.1:g.150426349C>T | GRCh37 |
| NC_000002.10:g.150134595C>T | NCBI36 |
| NG_009189.1:g.22982G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303319.10:c.*139G>A MANE Select | ENSP00000301920.5:n.*139G>A | |
| ENST00000303319.9:c.*139G>A | ENSP00000301920.5:n.*139G>A | |
| ENST00000422782.2:c.*139G>A | ENSP00000408331.2:n.*139G>A | |
| ENST00000428879.5:c.*139G>A | ENSP00000389060.1:n.*139G>A | |
| NM_015702.2:c.*139G>A | NP_056517.1:n.*139G>A | |
| NM_015702.3:c.*139G>A MANE Select | NP_056517.1:n.*139G>A |