Canonical Allele Identifier: CA377146160
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs1400643390

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72007747A>G , CM000672.2:g.72007747A>G GRCh38
NC_000010.10:g.73767505A>G , CM000672.1:g.73767505A>G GRCh37
NC_000010.9:g.73437511A>G NCBI36
NG_012635.1:g.48386A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.716A>G MANE Select ENSP00000362207.4:p.Lys239Arg
ENST00000373115.4:c.716A>G ENSP00000362207.4:p.Lys239Arg
NM_004273.4:c.716A>G NP_004264.2:p.Lys239Arg
XM_006718075.2:c.716A>G XP_006718138.1:p.Lys239Arg
XM_011540369.1:c.716A>G XP_011538671.1:p.Lys239Arg
XM_006718075.4:c.716A>G XP_006718138.1:p.Lys239Arg
XM_011540369.2:c.716A>G XP_011538671.1:p.Lys239Arg
NM_004273.5:c.716A>G MANE Select NP_004264.2:p.Lys239Arg