Canonical Allele Identifier: CA396790477

Gene: CHST6

Linked Data

• dbSNP Id: rs1399842810
• gnomAD v2: 16-75513077-G-A
• gnomAD v4: 16-75479179-G-A
• MyVariant Identifiers: chr16:g.75513077G>A (hg19) ; chr16:g.75479179G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479179G>A , CM000678.2:g.75479179G>A	GRCh38
NC_000016.9:g.75513077G>A , CM000678.1:g.75513077G>A	GRCh37
NC_000016.8:g.74070578G>A	NCBI36
NG_016442.1:g.20850C>T
NG_016442.2:g.21263C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.650C>T MANE Select	ENSP00000328983.4:p.Ala217Val
ENST00000390664.3:c.650C>T	ENSP00000375079.2:p.Ala217Val
ENST00000649341.1:c.650C>T	ENSP00000497635.1:p.Ala217Val
ENST00000649824.1:c.650C>T	ENSP00000496806.1:p.Ala217Val
ENST00000332272.8:c.650C>T	ENSP00000328983.4:p.Ala217Val
ENST00000390664.2:c.650C>T	ENSP00000375079.2:p.Ala217Val
NM_021615.4:c.650C>T	NP_067628.1:p.Ala217Val
XM_005255955.3:c.650C>T	XP_005256012.1:p.Ala217Val
XM_011523085.1:c.650C>T	XP_011521387.1:p.Ala217Val
NM_021615.5:c.650C>T MANE Select	NP_067628.1:p.Ala217Val
XM_005255955.5:c.650C>T	XP_005256012.1:p.Ala217Val
XM_011523085.3:c.650C>T	XP_011521387.1:p.Ala217Val
NR_163480.1:n.733+2638C>T
NR_163481.1:n.577+2638C>T