Linked Data
MyVariant Identifiers:
chr14:g.50597256A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50130538A>T , CM000676.2:g.50130538A>T | GRCh38 |
| NC_000014.8:g.50597256A>T , CM000676.1:g.50597256A>T | GRCh37 |
| NC_000014.7:g.49667006A>T | NCBI36 |
| NG_051073.1:g.106156T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216373.10:c.3300T>A MANE Select | ENSP00000216373.5:p.Leu1100= | |
| ENST00000216373.9:c.3300T>A | ENSP00000216373.5:p.Leu1100= | |
| ENST00000543680.5:c.3201T>A | ENSP00000445328.1:p.Leu1067= | |
| NM_006939.2:c.3300T>A | NP_008870.2:p.Leu1100= | |
| XM_005268021.1:c.3120T>A | XP_005268078.1:p.Leu1040= | |
| XM_011537103.1:c.3261T>A | XP_011535405.1:p.Leu1087= | |
| NM_006939.3:c.3300T>A | NP_008870.2:p.Leu1100= | |
| NM_006939.4:c.3300T>A MANE Select | NP_008870.2:p.Leu1100= |