Linked Data
MyVariant Identifiers:
chr14:g.60976656A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.60509938A>T , CM000676.2:g.60509938A>T | GRCh38 |
| NC_000014.8:g.60976656A>T , CM000676.1:g.60976656A>T | GRCh37 |
| NC_000014.7:g.60046409A>T | NCBI36 |
| NG_008203.1:g.5719A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000327720.6:c.540A>T (SIX6) MANE Select | ENSP00000328596.5:p.Arg180= | |
| ENST00000327720.5:c.540A>T (SIX6) | ENSP00000328596.5:p.Arg180= | |
| ENST00000556799.1:c.-144+5457T>A (C14orf39) | ENSP00000451441.1:n.-144+5457T>A | |
| NM_007374.2:c.540A>T (SIX6) | NP_031400.2:p.Arg180= | |
| NM_007374.3:c.540A>T (SIX6) MANE Select | NP_031400.2:p.Arg180= |