Linked Data
MyVariant Identifiers:
chr14:g.61115404G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.60648686G>T , CM000676.2:g.60648686G>T | GRCh38 |
| NC_000014.8:g.61115404G>T , CM000676.1:g.61115404G>T | GRCh37 |
| NC_000014.7:g.60185157G>T | NCBI36 |
| NG_008231.1:g.5752C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645694.3:c.504C>A (SIX1) MANE Select | ENSP00000494686.1:p.Val168= | |
| ENST00000247182.6:c.504C>A (SIX1) | ENSP00000247182.5:p.Val168= | |
| ENST00000553535.2:n.249-2109C>A (SIX1) | ||
| ENST00000554986.2:c.42-2109C>A (SIX1) | ENSP00000452700.2:n.42-2109C>A | |
| ENST00000555955.3:n.1198-2109C>A (SIX1) | ||
| NM_005982.3:c.504C>A (SIX1) | NP_005973.1:p.Val168= | |
| XM_017021602.2:c.501+3C>A (SIX1) | XP_016877091.1:n.501+3C>A | |
| NM_005982.4:c.504C>A (SIX1) MANE Select | NP_005973.1:p.Val168= | |
| NR_162089.1:n.39G>T (MIR9718) |