Canonical Allele Identifier: CA377145706

Gene: CHST3

Linked Data

• dbSNP Id: rs1287816179
• gnomAD v2: 10-73767456-G-C
• gnomAD v4: 10-72007698-G-C
• MyVariant Identifiers: chr10:g.73767456G>C (hg19) ; chr10:g.72007698G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72007698G>C , CM000672.2:g.72007698G>C	GRCh38
NC_000010.10:g.73767456G>C , CM000672.1:g.73767456G>C	GRCh37
NC_000010.9:g.73437462G>C	NCBI36
NG_012635.1:g.48337G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.667G>C MANE Select	ENSP00000362207.4:p.Gly223Arg
ENST00000373115.4:c.667G>C	ENSP00000362207.4:p.Gly223Arg
NM_004273.4:c.667G>C	NP_004264.2:p.Gly223Arg
XM_006718075.2:c.667G>C	XP_006718138.1:p.Gly223Arg
XM_011540369.1:c.667G>C	XP_011538671.1:p.Gly223Arg
XM_006718075.4:c.667G>C	XP_006718138.1:p.Gly223Arg
XM_011540369.2:c.667G>C	XP_011538671.1:p.Gly223Arg
NM_004273.5:c.667G>C MANE Select	NP_004264.2:p.Gly223Arg