Canonical Allele Identifier: CA377145456
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs371650865

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007665G>T , CM000672.2:g.72007665G>T GRCh38
NC_000010.10:g.73767423G>T , CM000672.1:g.73767423G>T GRCh37
NC_000010.9:g.73437429G>T NCBI36
NG_012635.1:g.48304G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.634G>T MANE Select ENSP00000362207.4:p.Glu212Ter
ENST00000373115.4:c.634G>T ENSP00000362207.4:p.Glu212Ter
NM_004273.4:c.634G>T NP_004264.2:p.Glu212Ter
XM_006718075.2:c.634G>T XP_006718138.1:p.Glu212Ter
XM_011540369.1:c.634G>T XP_011538671.1:p.Glu212Ter
XM_006718075.4:c.634G>T XP_006718138.1:p.Glu212Ter
XM_011540369.2:c.634G>T XP_011538671.1:p.Glu212Ter
NM_004273.5:c.634G>T MANE Select NP_004264.2:p.Glu212Ter