Linked Data
MyVariant Identifiers:
chr14:g.51376792C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.50910074C>T , CM000676.2:g.50910074C>T | GRCh38 |
| NC_000014.8:g.51376792C>T , CM000676.1:g.51376792C>T | GRCh37 |
| NC_000014.7:g.50446542C>T | NCBI36 |
| NG_012796.1:g.39457G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216392.8:c.1998G>A MANE Select | ENSP00000216392.7:p.Gln666= | |
| ENST00000216392.7:c.1998G>A | ENSP00000216392.7:p.Gln666= | |
| ENST00000532107.2:n.171G>A | ||
| ENST00000532462.5:c.1998G>A | ENSP00000431657.1:p.Gln666= | |
| ENST00000544180.6:c.1896G>A | ENSP00000443787.1:p.Gln632= | |
| NM_001163940.1:c.1896G>A | NP_001157412.1:p.Gln632= | |
| NM_002863.4:c.1998G>A | NP_002854.3:p.Gln666= | |
| NM_002863.5:c.1998G>A MANE Select | NP_002854.3:p.Gln666= | |
| NM_001163940.2:c.1896G>A | NP_001157412.1:p.Gln632= |