Canonical Allele Identifier: CA396789799
Gene: CHST6 HGNC NCBI

Linked Data

dbSNP Id: rs769174133

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.75479023C>T , CM000678.2:g.75479023C>T GRCh38
NC_000016.9:g.75512921C>T , CM000678.1:g.75512921C>T GRCh37
NC_000016.8:g.74070422C>T NCBI36
NG_016442.1:g.21006G>A
NG_016442.2:g.21419G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332272.9:c.806G>A MANE Select ENSP00000328983.4:p.Arg269His
ENST00000390664.3:c.806G>A ENSP00000375079.2:p.Arg269His
ENST00000649341.1:c.806G>A ENSP00000497635.1:p.Arg269His
ENST00000649824.1:c.806G>A ENSP00000496806.1:p.Arg269His
ENST00000332272.8:c.806G>A ENSP00000328983.4:p.Arg269His
ENST00000390664.2:c.806G>A ENSP00000375079.2:p.Arg269His
NM_021615.4:c.806G>A NP_067628.1:p.Arg269His
XM_005255955.3:c.806G>A XP_005256012.1:p.Arg269His
XM_011523085.1:c.806G>A XP_011521387.1:p.Arg269His
NM_021615.5:c.806G>A MANE Select NP_067628.1:p.Arg269His
XM_005255955.5:c.806G>A XP_005256012.1:p.Arg269His
XM_011523085.3:c.806G>A XP_011521387.1:p.Arg269His
NR_163480.1:n.733+2794G>A
NR_163481.1:n.577+2794G>A