Canonical Allele Identifier: CA377151909

Gene: CHST3

Linked Data

• dbSNP Id: rs1252780163
• gnomAD v2: 10-73768042-A-C
• gnomAD v4: 10-72008284-A-C
• MyVariant Identifiers: chr10:g.73768042A>C (hg19) ; chr10:g.72008284A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72008284A>C , CM000672.2:g.72008284A>C	GRCh38
NC_000010.10:g.73768042A>C , CM000672.1:g.73768042A>C	GRCh37
NC_000010.9:g.73438048A>C	NCBI36
NG_012635.1:g.48923A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.1253A>C MANE Select	ENSP00000362207.4:p.Gln418Pro
ENST00000373115.4:c.1253A>C	ENSP00000362207.4:p.Gln418Pro
NM_004273.4:c.1253A>C	NP_004264.2:p.Gln418Pro
XM_006718075.2:c.1253A>C	XP_006718138.1:p.Gln418Pro
XM_011540369.1:c.1253A>C	XP_011538671.1:p.Gln418Pro
XM_006718075.4:c.1253A>C	XP_006718138.1:p.Gln418Pro
XM_011540369.2:c.1253A>C	XP_011538671.1:p.Gln418Pro
NM_004273.5:c.1253A>C MANE Select	NP_004264.2:p.Gln418Pro