Linked Data
MyVariant Identifiers:
chr19:g.15990176A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15879366A>T , CM000681.2:g.15879366A>T | GRCh38 |
| NC_000019.9:g.15990176A>T , CM000681.1:g.15990176A>T | GRCh37 |
| NC_000019.8:g.15851176A>T | NCBI36 |
| NG_007971.2:g.23709T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000221700.11:c.1377T>A MANE Select | ENSP00000221700.3:p.Ile459= | |
| ENST00000011989.11:c.1377T>A | ENSP00000011989.8:p.Ile459= | |
| ENST00000221700.10:c.1377T>A | ENSP00000221700.3:p.Ile459= | |
| ENST00000392846.7:n.1320T>A | ||
| ENST00000589654.2:c.165T>A | ||
| NM_001082.4:c.1377T>A | NP_001073.3:p.Ile459= | |
| NM_001082.5:c.1377T>A MANE Select | NP_001073.3:p.Ile459= |