Canonical Allele Identifier: CA406420639
Gene: SIX5 HGNC NCBI

Linked Data

dbSNP Id: rs541085479
gnomAD v3: 19-45766965-C-A
gnomAD v4: 19-45766965-C-A
MyVariant Identifiers: chr19:g.46270223C>A (hg19) chr19:g.45766965C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766965C>A , CM000681.2:g.45766965C>A GRCh38
NC_000019.9:g.46270223C>A , CM000681.1:g.46270223C>A GRCh37
NC_000019.8:g.50962063C>A NCBI36
NG_012745.1:g.7275G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000317578.7:c.994G>T MANE Select ENSP00000316842.4:p.Gly332Cys
ENST00000317578.6:c.994G>T ENSP00000316842.4:p.Gly332Cys
ENST00000560160.1:c.587-854G>T
ENST00000560168.1:c.*182G>T ENSP00000453189.2:n.*182G>T
ENST00000622857.1:c.16-1003G>T ENSP00000481365.1:n.16-1003G>T
NM_175875.4:c.994G>T NP_787071.2:p.Gly332Cys
NM_175875.5:c.994G>T MANE Select NP_787071.3:p.Gly332Cys
Search 100 bp 5'
Search 100 bp 3'