Canonical Allele Identifier: CA396790572

Gene: CHST6

Linked Data

• gnomAD v4: 16-75479203-C-G
• MyVariant Identifiers: chr16:g.75513101C>G (hg19) ; chr16:g.75479203C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479203C>G , CM000678.2:g.75479203C>G	GRCh38
NC_000016.9:g.75513101C>G , CM000678.1:g.75513101C>G	GRCh37
NC_000016.8:g.74070602C>G	NCBI36
NG_016442.1:g.20826G>C
NG_016442.2:g.21239G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.626G>C MANE Select	ENSP00000328983.4:p.Arg209Pro
ENST00000390664.3:c.626G>C	ENSP00000375079.2:p.Arg209Pro
ENST00000649341.1:c.626G>C	ENSP00000497635.1:p.Arg209Pro
ENST00000649824.1:c.626G>C	ENSP00000496806.1:p.Arg209Pro
ENST00000332272.8:c.626G>C	ENSP00000328983.4:p.Arg209Pro
ENST00000390664.2:c.626G>C	ENSP00000375079.2:p.Arg209Pro
NM_021615.4:c.626G>C	NP_067628.1:p.Arg209Pro
XM_005255955.3:c.626G>C	XP_005256012.1:p.Arg209Pro
XM_011523085.1:c.626G>C	XP_011521387.1:p.Arg209Pro
NM_021615.5:c.626G>C MANE Select	NP_067628.1:p.Arg209Pro
XM_005255955.5:c.626G>C	XP_005256012.1:p.Arg209Pro
XM_011523085.3:c.626G>C	XP_011521387.1:p.Arg209Pro
NR_163480.1:n.733+2614G>C
NR_163481.1:n.577+2614G>C