Canonical Allele Identifier: CA377146879
Gene: CHST3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007841G>A , CM000672.2:g.72007841G>A GRCh38
NC_000010.10:g.73767599G>A , CM000672.1:g.73767599G>A GRCh37
NC_000010.9:g.73437605G>A NCBI36
NG_012635.1:g.48480G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.810G>A MANE Select ENSP00000362207.4:p.Met270Ile
ENST00000373115.4:c.810G>A ENSP00000362207.4:p.Met270Ile
NM_004273.4:c.810G>A NP_004264.2:p.Met270Ile
XM_006718075.2:c.810G>A XP_006718138.1:p.Met270Ile
XM_011540369.1:c.810G>A XP_011538671.1:p.Met270Ile
XM_006718075.4:c.810G>A XP_006718138.1:p.Met270Ile
XM_011540369.2:c.810G>A XP_011538671.1:p.Met270Ile
NM_004273.5:c.810G>A MANE Select NP_004264.2:p.Met270Ile