Canonical Allele Identifier: CA406420880
Gene: SIX5 HGNC NCBI

Linked Data

dbSNP Id: rs1969091742
COSMIC: COSM6373355
MyVariant Identifiers: chr19:g.46270273C>A (hg19) chr19:g.45767015C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45767015C>A , CM000681.2:g.45767015C>A GRCh38
NC_000019.9:g.46270273C>A , CM000681.1:g.46270273C>A GRCh37
NC_000019.8:g.50962113C>A NCBI36
NG_012745.1:g.7225G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.944G>T MANE Select ENSP00000316842.4:p.Cys315Phe
ENST00000317578.6:c.944G>T ENSP00000316842.4:p.Cys315Phe
ENST00000560160.1:c.587-904G>T
ENST00000560168.1:c.*132G>T ENSP00000453189.2:n.*132G>T
ENST00000622857.1:c.16-1053G>T ENSP00000481365.1:n.16-1053G>T
NM_175875.4:c.944G>T NP_787071.2:p.Cys315Phe
NM_175875.5:c.944G>T MANE Select NP_787071.3:p.Cys315Phe
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