Linked Data
gnomAD v4:
3-119413738-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119413738T>A , CM000665.2:g.119413738T>A | GRCh38 |
| NC_000003.11:g.119132585T>A , CM000665.1:g.119132585T>A | GRCh37 |
| NC_000003.10:g.120615275T>A | NCBI36 |
| NG_007665.2:g.124366T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.1927-118T>A MANE Select | ENSP00000264245.4:n.1927-118T>A | |
| ENST00000264245.8:c.1927-118T>A | ENSP00000264245.4:n.1927-118T>A | |
| NM_020754.3:c.1927-118T>A | NP_065805.2:n.1927-118T>A | |
| XM_005247671.3:c.1834-118T>A | XP_005247728.1:n.1834-118T>A | |
| XM_006713714.2:c.1867-118T>A | XP_006713777.1:n.1867-118T>A | |
| XM_006713714.3:c.1867-118T>A | XP_006713777.1:n.1867-118T>A | |
| XM_017006955.1:c.1435-118T>A | XP_016862444.1:n.1435-118T>A | |
| NM_020754.4:c.1927-118T>A MANE Select | NP_065805.2:n.1927-118T>A |