Linked Data
MyVariant Identifiers:
chr14:g.29236842T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.28767636T>C , CM000676.2:g.28767636T>C | GRCh38 |
| NC_000014.8:g.29236842T>C , CM000676.1:g.29236842T>C | GRCh37 |
| NC_000014.7:g.28306593T>C | NCBI36 |
| NG_009367.1:g.5556T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706482.1:c.357T>C | ENSP00000516406.1:p.Ala119= | |
| ENST00000313071.7:c.357T>C MANE Select | ENSP00000339004.3:p.Ala119= | |
| ENST00000313071.6:c.357T>C | ENSP00000339004.3:p.Ala119= | |
| NM_005249.4:c.357T>C | NP_005240.3:p.Ala119= | |
| NM_005249.5:c.357T>C MANE Select | NP_005240.3:p.Ala119= |