Canonical Allele Identifier: CA396790690

Gene: CHST6

Linked Data

• dbSNP Id: rs1334965451
• gnomAD v2: 16-75513134-A-G
• gnomAD v4: 16-75479236-A-G
• MyVariant Identifiers: chr16:g.75513134A>G (hg19) ; chr16:g.75479236A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.75479236A>G , CM000678.2:g.75479236A>G	GRCh38
NC_000016.9:g.75513134A>G , CM000678.1:g.75513134A>G	GRCh37
NC_000016.8:g.74070635A>G	NCBI36
NG_016442.1:g.20793T>C
NG_016442.2:g.21206T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332272.9:c.593T>C MANE Select	ENSP00000328983.4:p.Val198Ala
ENST00000390664.3:c.593T>C	ENSP00000375079.2:p.Val198Ala
ENST00000649341.1:c.593T>C	ENSP00000497635.1:p.Val198Ala
ENST00000649824.1:c.593T>C	ENSP00000496806.1:p.Val198Ala
ENST00000332272.8:c.593T>C	ENSP00000328983.4:p.Val198Ala
ENST00000390664.2:c.593T>C	ENSP00000375079.2:p.Val198Ala
NM_021615.4:c.593T>C	NP_067628.1:p.Val198Ala
XM_005255955.3:c.593T>C	XP_005256012.1:p.Val198Ala
XM_011523085.1:c.593T>C	XP_011521387.1:p.Val198Ala
NM_021615.5:c.593T>C MANE Select	NP_067628.1:p.Val198Ala
XM_005255955.5:c.593T>C	XP_005256012.1:p.Val198Ala
XM_011523085.3:c.593T>C	XP_011521387.1:p.Val198Ala
NR_163480.1:n.733+2581T>C
NR_163481.1:n.577+2581T>C