Canonical Allele Identifier: CA377151629
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs1840067873

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008226G>C , CM000672.2:g.72008226G>C GRCh38
NC_000010.10:g.73767984G>C , CM000672.1:g.73767984G>C GRCh37
NC_000010.9:g.73437990G>C NCBI36
NG_012635.1:g.48865G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1195G>C MANE Select ENSP00000362207.4:p.Asp399His
ENST00000373115.4:c.1195G>C ENSP00000362207.4:p.Asp399His
NM_004273.4:c.1195G>C NP_004264.2:p.Asp399His
XM_006718075.2:c.1195G>C XP_006718138.1:p.Asp399His
XM_011540369.1:c.1195G>C XP_011538671.1:p.Asp399His
XM_006718075.4:c.1195G>C XP_006718138.1:p.Asp399His
XM_011540369.2:c.1195G>C XP_011538671.1:p.Asp399His
NM_004273.5:c.1195G>C MANE Select NP_004264.2:p.Asp399His