Canonical Allele Identifier: CA470283753
Gene: CHST3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.73767299C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007541C>G , CM000672.2:g.72007541C>G GRCh38
NC_000010.10:g.73767299C>G , CM000672.1:g.73767299C>G GRCh37
NC_000010.9:g.73437305C>G NCBI36
NG_012635.1:g.48180C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.510C>G MANE Select ENSP00000362207.4:p.Arg170=
ENST00000373115.4:c.510C>G ENSP00000362207.4:p.Arg170=
NM_004273.4:c.510C>G NP_004264.2:p.Arg170=
XM_006718075.2:c.510C>G XP_006718138.1:p.Arg170=
XM_011540369.1:c.510C>G XP_011538671.1:p.Arg170=
XM_006718075.4:c.510C>G XP_006718138.1:p.Arg170=
XM_011540369.2:c.510C>G XP_011538671.1:p.Arg170=
NM_004273.5:c.510C>G MANE Select NP_004264.2:p.Arg170=