Canonical Allele Identifier: CA377151603

Gene: CHST3

Linked Data

• dbSNP Id: rs995382252
• gnomAD v3: 10-72008221-T-C
• gnomAD v4: 10-72008221-T-C
• MyVariant Identifiers: chr10:g.73767979T>C (hg19) ; chr10:g.72008221T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.72008221T>C , CM000672.2:g.72008221T>C	GRCh38
NC_000010.10:g.73767979T>C , CM000672.1:g.73767979T>C	GRCh37
NC_000010.9:g.73437985T>C	NCBI36
NG_012635.1:g.48860T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373115.5:c.1190T>C MANE Select	ENSP00000362207.4:p.Val397Ala
ENST00000373115.4:c.1190T>C	ENSP00000362207.4:p.Val397Ala
NM_004273.4:c.1190T>C	NP_004264.2:p.Val397Ala
XM_006718075.2:c.1190T>C	XP_006718138.1:p.Val397Ala
XM_011540369.1:c.1190T>C	XP_011538671.1:p.Val397Ala
XM_006718075.4:c.1190T>C	XP_006718138.1:p.Val397Ala
XM_011540369.2:c.1190T>C	XP_011538671.1:p.Val397Ala
NM_004273.5:c.1190T>C MANE Select	NP_004264.2:p.Val397Ala