Canonical Allele Identifier: CA396790248

Gene: CHST6

Linked Data

• gnomAD v4: 16-75479120-G-T
• MyVariant Identifiers: chr16:g.75513018G>T (hg19) ; chr16:g.75479120G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479120G>T , CM000678.2:g.75479120G>T	GRCh38
NC_000016.9:g.75513018G>T , CM000678.1:g.75513018G>T	GRCh37
NC_000016.8:g.74070519G>T	NCBI36
NG_016442.1:g.20909C>A
NG_016442.2:g.21322C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.709C>A MANE Select	ENSP00000328983.4:p.Pro237Thr
ENST00000390664.3:c.709C>A	ENSP00000375079.2:p.Pro237Thr
ENST00000649341.1:c.709C>A	ENSP00000497635.1:p.Pro237Thr
ENST00000649824.1:c.709C>A	ENSP00000496806.1:p.Pro237Thr
ENST00000332272.8:c.709C>A	ENSP00000328983.4:p.Pro237Thr
ENST00000390664.2:c.709C>A	ENSP00000375079.2:p.Pro237Thr
NM_021615.4:c.709C>A	NP_067628.1:p.Pro237Thr
XM_005255955.3:c.709C>A	XP_005256012.1:p.Pro237Thr
XM_011523085.1:c.709C>A	XP_011521387.1:p.Pro237Thr
NM_021615.5:c.709C>A MANE Select	NP_067628.1:p.Pro237Thr
XM_005255955.5:c.709C>A	XP_005256012.1:p.Pro237Thr
XM_011523085.3:c.709C>A	XP_011521387.1:p.Pro237Thr
NR_163480.1:n.733+2697C>A
NR_163481.1:n.577+2697C>A