Canonical Allele Identifier: CA496693888

Gene: CHST6

Linked Data

• gnomAD v4: 16-75479313-C-A
• MyVariant Identifiers: chr16:g.75513211C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479313C>A , CM000678.2:g.75479313C>A	GRCh38
NC_000016.9:g.75513211C>A , CM000678.1:g.75513211C>A	GRCh37
NC_000016.8:g.74070712C>A	NCBI36
NG_016442.1:g.20716G>T
NG_016442.2:g.21129G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.516G>T MANE Select	ENSP00000328983.4:p.Val172=
ENST00000390664.3:c.516G>T	ENSP00000375079.2:p.Val172=
ENST00000649341.1:c.516G>T	ENSP00000497635.1:p.Val172=
ENST00000649824.1:c.516G>T	ENSP00000496806.1:p.Val172=
ENST00000332272.8:c.516G>T	ENSP00000328983.4:p.Val172=
ENST00000390664.2:c.516G>T	ENSP00000375079.2:p.Val172=
NM_021615.4:c.516G>T	NP_067628.1:p.Val172=
XM_005255955.3:c.516G>T	XP_005256012.1:p.Val172=
XM_011523085.1:c.516G>T	XP_011521387.1:p.Val172=
NM_021615.5:c.516G>T MANE Select	NP_067628.1:p.Val172=
XM_005255955.5:c.516G>T	XP_005256012.1:p.Val172=
XM_011523085.3:c.516G>T	XP_011521387.1:p.Val172=
NR_163480.1:n.733+2504G>T
NR_163481.1:n.577+2504G>T