Canonical Allele Identifier: CA1918976172
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007718C= , CM000672.2:g.72007718C= GRCh38
NC_000010.10:g.73767476C= , CM000672.1:g.73767476C= GRCh37
NC_000010.9:g.73437482C= NCBI36
NG_012635.1:g.48357C=

Transcript Alleles

HGVS Amino-acid change
ENST00000373115.5:c.687C= MANE Select ENSP00000362207.4:p.Cys229=
ENST00000373115.4:c.687C= ENSP00000362207.4:p.Cys229=
NM_004273.4:c.687C= NP_004264.2:p.Cys229=
XM_006718075.2:c.687C= XP_006718138.1:p.Cys229=
XM_011540369.1:c.687C= XP_011538671.1:p.Cys229=
XM_006718075.4:c.687C= XP_006718138.1:p.Cys229=
XM_011540369.2:c.687C= XP_011538671.1:p.Cys229=
NM_004273.5:c.687C= MANE Select NP_004264.2:p.Cys229=