Canonical Allele Identifier: CA406419909
Gene: SIX5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.46270201T>G (hg19) chr19:g.45766943T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766943T>G , CM000681.2:g.45766943T>G GRCh38
NC_000019.9:g.46270201T>G , CM000681.1:g.46270201T>G GRCh37
NC_000019.8:g.50962041T>G NCBI36
NG_012745.1:g.7297A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1016A>C MANE Select ENSP00000316842.4:p.Asn339Thr
ENST00000317578.6:c.1016A>C ENSP00000316842.4:p.Asn339Thr
ENST00000560160.1:c.587-832A>C
ENST00000560168.1:c.*204A>C ENSP00000453189.2:n.*204A>C
ENST00000622857.1:c.16-981A>C ENSP00000481365.1:n.16-981A>C
NM_175875.4:c.1016A>C NP_787071.2:p.Asn339Thr
NM_175875.5:c.1016A>C MANE Select NP_787071.3:p.Asn339Thr
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