Canonical Allele Identifier: CA2658868997

Gene: SIX3

Linked Data

• gnomAD v4: 2-44942023-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.44942023T>G , CM000664.2:g.44942023T>G	GRCh38
NC_000002.11:g.45169162T>G , CM000664.1:g.45169162T>G	GRCh37
NC_000002.10:g.45022666T>G	NCBI36
NG_016222.1:g.5126T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260653.5:c.-82T>G MANE Select	ENSP00000260653.3:n.-82T>G
ENST00000260653.4:c.-82T>G	ENSP00000260653.3:n.-82T>G
NM_005413.3:c.-82T>G	NP_005404.1:n.-82T>G
XM_011533042.1:c.-82T>G	XP_011531344.1:n.-82T>G
NM_005413.4:c.-82T>G MANE Select	NP_005404.1:n.-82T>G