Canonical Allele Identifier: CA628886539

Gene: CHST9

Linked Data

• dbSNP Id: rs1246248823
• gnomAD v2: 18-24570675-G-A
• gnomAD v3: 18-26990711-G-A
• gnomAD v4: 18-26990711-G-A
• MyVariant Identifiers: chr18:g.24570675G>A (hg19) ; chr18:g.26990711G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.26990711G>A , CM000680.2:g.26990711G>A	GRCh38
NC_000018.9:g.24570675G>A , CM000680.1:g.24570675G>A	GRCh37
NC_000018.8:g.22824673G>A	NCBI36
NG_029856.1:g.199615C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000618847.5:c.202+33405C>T MANE Select	ENSP00000480991.1:n.202+33405C>T
ENST00000284224.9:c.-16+33405C>T	ENSP00000284224.9:n.-16+33405C>T
ENST00000580774.2:c.202+33405C>T	ENSP00000464655.1:n.202+33405C>T
ENST00000581714.5:c.202+33405C>T	ENSP00000462852.1:n.202+33405C>T
ENST00000618847.4:c.202+33405C>T	ENSP00000480991.1:n.202+33405C>T
NM_001256316.1:c.202+33405C>T	NP_001243245.1:n.202+33405C>T
NM_031422.5:c.202+33405C>T	NP_113610.2:n.202+33405C>T
XM_006722555.2:c.202+33405C>T	XP_006722618.1:n.202+33405C>T
XM_011526225.1:c.1+33405C>T	XP_011524527.1:n.1+33405C>T
XM_006722555.4:c.202+33405C>T	XP_006722618.1:n.202+33405C>T
XM_017026033.1:c.202+33405C>T	XP_016881522.1:n.202+33405C>T
XM_017026034.1:c.-66-11959C>T	XP_016881523.1:n.-66-11959C>T
NM_031422.6:c.202+33405C>T MANE Select	NP_113610.2:n.202+33405C>T
NM_001256316.2:c.202+33405C>T	NP_001243245.1:n.202+33405C>T
NM_001398493.1:c.202+33405C>T	NP_001385422.1:n.202+33405C>T