Canonical Allele Identifier: CA507961362
Gene: SIX5 HGNC NCBI

Linked Data

gnomAD v4: 19-45766705-T-G
MyVariant Identifiers: chr19:g.46269963T>G (hg19)
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Genomic Alleles

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

Transcript Alleles

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