Canonical Allele Identifier: CA377147153
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs1220584098

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007872G>A , CM000672.2:g.72007872G>A GRCh38
NC_000010.10:g.73767630G>A , CM000672.1:g.73767630G>A GRCh37
NC_000010.9:g.73437636G>A NCBI36
NG_012635.1:g.48511G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.841G>A MANE Select ENSP00000362207.4:p.Glu281Lys
ENST00000373115.4:c.841G>A ENSP00000362207.4:p.Glu281Lys
NM_004273.4:c.841G>A NP_004264.2:p.Glu281Lys
XM_006718075.2:c.841G>A XP_006718138.1:p.Glu281Lys
XM_011540369.1:c.841G>A XP_011538671.1:p.Glu281Lys
XM_006718075.4:c.841G>A XP_006718138.1:p.Glu281Lys
XM_011540369.2:c.841G>A XP_011538671.1:p.Glu281Lys
NM_004273.5:c.841G>A MANE Select NP_004264.2:p.Glu281Lys