Canonical Allele Identifier: CA2722110471
Gene: CHST3 HGNC NCBI

Linked Data

dbSNP Id: rs2131778446
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009359A>G , CM000672.2:g.72009359A>G GRCh38
NC_000010.10:g.73769117A>G , CM000672.1:g.73769117A>G GRCh37
NC_000010.9:g.73439123A>G NCBI36
NG_012635.1:g.49998A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*888A>G MANE Select ENSP00000362207.4:n.*888A>G
ENST00000373115.4:c.*888A>G ENSP00000362207.4:n.*888A>G
NM_004273.4:c.*888A>G NP_004264.2:n.*888A>G
XM_006718075.2:c.*888A>G XP_006718138.1:n.*888A>G
XM_011540369.1:c.*888A>G XP_011538671.1:n.*888A>G
XM_006718075.4:c.*888A>G XP_006718138.1:n.*888A>G
XM_011540369.2:c.*888A>G XP_011538671.1:n.*888A>G
NM_004273.5:c.*888A>G MANE Select NP_004264.2:n.*888A>G
Search 100 bp 5'
Search 100 bp 3'