Canonical Allele Identifier: CA406417592

Gene: SIX5

Linked Data

• dbSNP Id: rs765592386
• gnomAD v4: 19-45766437-C-T
• MyVariant Identifiers: chr19:g.46269695C>T (hg19) ; chr19:g.45766437C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.45766437C>T , CM000681.2:g.45766437C>T	GRCh38
NC_000019.9:g.46269695C>T , CM000681.1:g.46269695C>T	GRCh37
NC_000019.8:g.50961535C>T	NCBI36
NG_012745.1:g.7803G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317578.7:c.1522G>A MANE Select	ENSP00000316842.4:p.Ala508Thr
ENST00000317578.6:c.1522G>A	ENSP00000316842.4:p.Ala508Thr
ENST00000560160.1:c.587-326G>A
ENST00000560168.1:c.*710G>A	ENSP00000453189.2:n.*710G>A
ENST00000622857.1:c.16-475G>A	ENSP00000481365.1:n.16-475G>A
NM_175875.4:c.1522G>A	NP_787071.2:p.Ala508Thr
NM_175875.5:c.1522G>A MANE Select	NP_787071.3:p.Ala508Thr