Canonical Allele Identifier: CA470283757
Gene: CHST3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.73767305G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007547G>A , CM000672.2:g.72007547G>A GRCh38
NC_000010.10:g.73767305G>A , CM000672.1:g.73767305G>A GRCh37
NC_000010.9:g.73437311G>A NCBI36
NG_012635.1:g.48186G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.516G>A MANE Select ENSP00000362207.4:p.Val172=
ENST00000373115.4:c.516G>A ENSP00000362207.4:p.Val172=
NM_004273.4:c.516G>A NP_004264.2:p.Val172=
XM_006718075.2:c.516G>A XP_006718138.1:p.Val172=
XM_011540369.1:c.516G>A XP_011538671.1:p.Val172=
XM_006718075.4:c.516G>A XP_006718138.1:p.Val172=
XM_011540369.2:c.516G>A XP_011538671.1:p.Val172=
NM_004273.5:c.516G>A MANE Select NP_004264.2:p.Val172=