Canonical Allele Identifier: CA486814147
Gene: SIX6 HGNC NCBI
C14orf39 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.60976614A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60509896A>C , CM000676.2:g.60509896A>C GRCh38
NC_000014.8:g.60976614A>C , CM000676.1:g.60976614A>C GRCh37
NC_000014.7:g.60046367A>C NCBI36
NG_008203.1:g.5677A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000327720.6:c.498A>C (SIX6) MANE Select ENSP00000328596.5:p.Gly166=
ENST00000327720.5:c.498A>C (SIX6) ENSP00000328596.5:p.Gly166=
ENST00000556799.1:c.-144+5499T>G (C14orf39) ENSP00000451441.1:n.-144+5499T>G
NM_007374.2:c.498A>C (SIX6) NP_031400.2:p.Gly166=
NM_007374.3:c.498A>C (SIX6) MANE Select NP_031400.2:p.Gly166=
Search 100 bp 5'
Search 100 bp 3'