Canonical Allele Identifier: CA2573778308
Gene: CHST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.72009222G>C , CM000672.2:g.72009222G>C GRCh38
NC_000010.10:g.73768980G>C , CM000672.1:g.73768980G>C GRCh37
NC_000010.9:g.73438986G>C NCBI36
NG_012635.1:g.49861G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373115.5:c.*751G>C MANE Select ENSP00000362207.4:n.*751G>C
ENST00000373115.4:c.*751G>C ENSP00000362207.4:n.*751G>C
NM_004273.4:c.*751G>C NP_004264.2:n.*751G>C
XM_006718075.2:c.*751G>C XP_006718138.1:n.*751G>C
XM_011540369.1:c.*751G>C XP_011538671.1:n.*751G>C
XM_006718075.4:c.*751G>C XP_006718138.1:n.*751G>C
XM_011540369.2:c.*751G>C XP_011538671.1:n.*751G>C
NM_004273.5:c.*751G>C MANE Select NP_004264.2:n.*751G>C