Canonical Allele Identifier: CA1918975856
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007535C= , CM000672.2:g.72007535C= GRCh38
NC_000010.10:g.73767293C= , CM000672.1:g.73767293C= GRCh37
NC_000010.9:g.73437299C= NCBI36
NG_012635.1:g.48174C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.504C= MANE Select ENSP00000362207.4:p.Ile168=
ENST00000373115.4:c.504C= ENSP00000362207.4:p.Ile168=
NM_004273.4:c.504C= NP_004264.2:p.Ile168=
XM_006718075.2:c.504C= XP_006718138.1:p.Ile168=
XM_011540369.1:c.504C= XP_011538671.1:p.Ile168=
XM_006718075.4:c.504C= XP_006718138.1:p.Ile168=
XM_011540369.2:c.504C= XP_011538671.1:p.Ile168=
NM_004273.5:c.504C= MANE Select NP_004264.2:p.Ile168=