Canonical Allele Identifier: CA377151901
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs1440763802

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72008283C>G , CM000672.2:g.72008283C>G GRCh38
NC_000010.10:g.73768041C>G , CM000672.1:g.73768041C>G GRCh37
NC_000010.9:g.73438047C>G NCBI36
NG_012635.1:g.48922C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.1252C>G MANE Select ENSP00000362207.4:p.Gln418Glu
ENST00000373115.4:c.1252C>G ENSP00000362207.4:p.Gln418Glu
NM_004273.4:c.1252C>G NP_004264.2:p.Gln418Glu
XM_006718075.2:c.1252C>G XP_006718138.1:p.Gln418Glu
XM_011540369.1:c.1252C>G XP_011538671.1:p.Gln418Glu
XM_006718075.4:c.1252C>G XP_006718138.1:p.Gln418Glu
XM_011540369.2:c.1252C>G XP_011538671.1:p.Gln418Glu
NM_004273.5:c.1252C>G MANE Select NP_004264.2:p.Gln418Glu