Canonical Allele Identifier: CA470283756
Gene: CHST3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.73767302A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007544A>T , CM000672.2:g.72007544A>T GRCh38
NC_000010.10:g.73767302A>T , CM000672.1:g.73767302A>T GRCh37
NC_000010.9:g.73437308A>T NCBI36
NG_012635.1:g.48183A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.513A>T MANE Select ENSP00000362207.4:p.Thr171=
ENST00000373115.4:c.513A>T ENSP00000362207.4:p.Thr171=
NM_004273.4:c.513A>T NP_004264.2:p.Thr171=
XM_006718075.2:c.513A>T XP_006718138.1:p.Thr171=
XM_011540369.1:c.513A>T XP_011538671.1:p.Thr171=
XM_006718075.4:c.513A>T XP_006718138.1:p.Thr171=
XM_011540369.2:c.513A>T XP_011538671.1:p.Thr171=
NM_004273.5:c.513A>T MANE Select NP_004264.2:p.Thr171=