Canonical Allele Identifier: CA406417752
Gene: SIX5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.46269730A>C (hg19) chr19:g.45766472A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766472A>C , CM000681.2:g.45766472A>C GRCh38
NC_000019.9:g.46269730A>C , CM000681.1:g.46269730A>C GRCh37
NC_000019.8:g.50961570A>C NCBI36
NG_012745.1:g.7768T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.1487T>G MANE Select ENSP00000316842.4:p.Leu496Arg
ENST00000317578.6:c.1487T>G ENSP00000316842.4:p.Leu496Arg
ENST00000560160.1:c.587-361T>G
ENST00000560168.1:c.*675T>G ENSP00000453189.2:n.*675T>G
ENST00000622857.1:c.16-510T>G ENSP00000481365.1:n.16-510T>G
NM_175875.4:c.1487T>G NP_787071.2:p.Leu496Arg
NM_175875.5:c.1487T>G MANE Select NP_787071.3:p.Leu496Arg
Search 100 bp 5'
Search 100 bp 3'