Canonical Allele Identifier: CA377145779
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs1240657101

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007707C>T , CM000672.2:g.72007707C>T GRCh38
NC_000010.10:g.73767465C>T , CM000672.1:g.73767465C>T GRCh37
NC_000010.9:g.73437471C>T NCBI36
NG_012635.1:g.48346C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.676C>T MANE Select ENSP00000362207.4:p.Arg226Cys
ENST00000373115.4:c.676C>T ENSP00000362207.4:p.Arg226Cys
NM_004273.4:c.676C>T NP_004264.2:p.Arg226Cys
XM_006718075.2:c.676C>T XP_006718138.1:p.Arg226Cys
XM_011540369.1:c.676C>T XP_011538671.1:p.Arg226Cys
XM_006718075.4:c.676C>T XP_006718138.1:p.Arg226Cys
XM_011540369.2:c.676C>T XP_011538671.1:p.Arg226Cys
NM_004273.5:c.676C>T MANE Select NP_004264.2:p.Arg226Cys