Canonical Allele Identifier: CA426126336

Gene: SIX3

Linked Data

• gnomAD v4: 2-44942221-A-T
• MyVariant Identifiers: chr2:g.45169360A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.44942221A>T , CM000664.2:g.44942221A>T	GRCh38
NC_000002.11:g.45169360A>T , CM000664.1:g.45169360A>T	GRCh37
NC_000002.10:g.45022864A>T	NCBI36
NG_016222.1:g.5324A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260653.5:c.117A>T MANE Select	ENSP00000260653.3:p.Gly39=
ENST00000260653.4:c.117A>T	ENSP00000260653.3:p.Gly39=
NM_005413.3:c.117A>T	NP_005404.1:p.Gly39=
XM_011533042.1:c.117A>T	XP_011531344.1:p.Gly39=
NM_005413.4:c.117A>T MANE Select	NP_005404.1:p.Gly39=