Canonical Allele Identifier: CA1918976032

Gene: CHST3

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72007649C= , CM000672.2:g.72007649C=	GRCh38
NC_000010.10:g.73767407C= , CM000672.1:g.73767407C=	GRCh37
NC_000010.9:g.73437413C=	NCBI36
NG_012635.1:g.48288C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.618C= MANE Select	ENSP00000362207.4:p.Phe206=
ENST00000373115.4:c.618C=	ENSP00000362207.4:p.Phe206=
NM_004273.4:c.618C=	NP_004264.2:p.Phe206=
XM_006718075.2:c.618C=	XP_006718138.1:p.Phe206=
XM_011540369.1:c.618C=	XP_011538671.1:p.Phe206=
XM_006718075.4:c.618C=	XP_006718138.1:p.Phe206=
XM_011540369.2:c.618C=	XP_011538671.1:p.Phe206=
NM_004273.5:c.618C= MANE Select	NP_004264.2:p.Phe206=