Canonical Allele Identifier: CA396792809

Gene: CHST6

Linked Data

• dbSNP Id: rs2080110231
• MyVariant Identifiers: chr16:g.75513306C>G (hg19) ; chr16:g.75479408C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479408C>G , CM000678.2:g.75479408C>G	GRCh38
NC_000016.9:g.75513306C>G , CM000678.1:g.75513306C>G	GRCh37
NC_000016.8:g.74070807C>G	NCBI36
NG_016442.1:g.20621G>C
NG_016442.2:g.21034G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.421G>C MANE Select	ENSP00000328983.4:p.Gly141Arg
ENST00000390664.3:c.421G>C	ENSP00000375079.2:p.Gly141Arg
ENST00000649341.1:c.421G>C	ENSP00000497635.1:p.Gly141Arg
ENST00000649824.1:c.421G>C	ENSP00000496806.1:p.Gly141Arg
ENST00000332272.8:c.421G>C	ENSP00000328983.4:p.Gly141Arg
ENST00000390664.2:c.421G>C	ENSP00000375079.2:p.Gly141Arg
NM_021615.4:c.421G>C	NP_067628.1:p.Gly141Arg
XM_005255955.3:c.421G>C	XP_005256012.1:p.Gly141Arg
XM_011523085.1:c.421G>C	XP_011521387.1:p.Gly141Arg
NM_021615.5:c.421G>C MANE Select	NP_067628.1:p.Gly141Arg
XM_005255955.5:c.421G>C	XP_005256012.1:p.Gly141Arg
XM_011523085.3:c.421G>C	XP_011521387.1:p.Gly141Arg
NR_163480.1:n.733+2409G>C
NR_163481.1:n.577+2409G>C