Canonical Allele Identifier: CA507961359
Gene: SIX5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2875569
ClinVar RCV Id: RCV003707301
gnomAD v4: 19-45766705-T-C
MyVariant Identifiers: chr19:g.46269963T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.45766705T>C , CM000681.2:g.45766705T>C GRCh38
NC_000019.9:g.46269963T>C , CM000681.1:g.46269963T>C GRCh37
NC_000019.8:g.50961803T>C NCBI36
NG_012745.1:g.7535A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000317578.7:c.1254A>G MANE Select ENSP00000316842.4:p.Gly418=
ENST00000317578.6:c.1254A>G ENSP00000316842.4:p.Gly418=
ENST00000560160.1:c.587-594A>G
ENST00000560168.1:c.*442A>G ENSP00000453189.2:n.*442A>G
ENST00000622857.1:c.16-743A>G ENSP00000481365.1:n.16-743A>G
NM_175875.4:c.1254A>G NP_787071.2:p.Gly418=
NM_175875.5:c.1254A>G MANE Select NP_787071.3:p.Gly418=
Search 100 bp 5'
Search 100 bp 3'