Canonical Allele Identifier: CA1918976032
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007649C= , CM000672.2:g.72007649C= GRCh38
NC_000010.10:g.73767407C= , CM000672.1:g.73767407C= GRCh37
NC_000010.9:g.73437413C= NCBI36
NG_012635.1:g.48288C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.618C= MANE Select ENSP00000362207.4:p.Phe206=
ENST00000373115.4:c.618C= ENSP00000362207.4:p.Phe206=
NM_004273.4:c.618C= NP_004264.2:p.Phe206=
XM_006718075.2:c.618C= XP_006718138.1:p.Phe206=
XM_011540369.1:c.618C= XP_011538671.1:p.Phe206=
XM_006718075.4:c.618C= XP_006718138.1:p.Phe206=
XM_011540369.2:c.618C= XP_011538671.1:p.Phe206=
NM_004273.5:c.618C= MANE Select NP_004264.2:p.Phe206=