Canonical Allele Identifier: CA496693817

Gene: CHST6

Linked Data

• MyVariant Identifiers: chr16:g.75512911G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479013G>C , CM000678.2:g.75479013G>C	GRCh38
NC_000016.9:g.75512911G>C , CM000678.1:g.75512911G>C	GRCh37
NC_000016.8:g.74070412G>C	NCBI36
NG_016442.1:g.21016C>G
NG_016442.2:g.21429C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000332272.9:c.816C>G MANE Select	ENSP00000328983.4:p.Arg272=
ENST00000390664.3:c.816C>G	ENSP00000375079.2:p.Arg272=
ENST00000649341.1:c.816C>G	ENSP00000497635.1:p.Arg272=
ENST00000649824.1:c.816C>G	ENSP00000496806.1:p.Arg272=
ENST00000332272.8:c.816C>G	ENSP00000328983.4:p.Arg272=
ENST00000390664.2:c.816C>G	ENSP00000375079.2:p.Arg272=
NM_021615.4:c.816C>G	NP_067628.1:p.Arg272=
XM_005255955.3:c.816C>G	XP_005256012.1:p.Arg272=
XM_011523085.1:c.816C>G	XP_011521387.1:p.Arg272=
NM_021615.5:c.816C>G MANE Select	NP_067628.1:p.Arg272=
XM_005255955.5:c.816C>G	XP_005256012.1:p.Arg272=
XM_011523085.3:c.816C>G	XP_011521387.1:p.Arg272=
NR_163480.1:n.733+2804C>G
NR_163481.1:n.577+2804C>G