Canonical Allele Identifier: CA14619708
Gene: CHST9 HGNC NCBI

Linked Data

dbSNP Id: rs9953270
gnomAD v2: 18-24687371-T-C
gnomAD v3: 18-27107407-T-C
gnomAD v4: 18-27107407-T-C
MyVariant Identifiers: chr18:g.24687371T>C (hg19) chr18:g.27107407T>C (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.27107407T>C , CM000680.2:g.27107407T>C GRCh38
NC_000018.9:g.24687371T>C , CM000680.1:g.24687371T>C GRCh37
NC_000018.8:g.22941369T>C NCBI36
NG_029856.1:g.82919A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000618847.5:c.121+35282A>G MANE Select ENSP00000480991.1:n.121+35282A>G
ENST00000580774.2:c.121+35282A>G ENSP00000464655.1:n.121+35282A>G
ENST00000581714.5:c.121+35282A>G ENSP00000462852.1:n.121+35282A>G
ENST00000618847.4:c.121+35282A>G ENSP00000480991.1:n.121+35282A>G
NM_001256316.1:c.121+35282A>G NP_001243245.1:n.121+35282A>G
NM_031422.5:c.121+35282A>G NP_113610.2:n.121+35282A>G
XM_006722555.2:c.121+35282A>G XP_006722618.1:n.121+35282A>G
XM_006722555.4:c.121+35282A>G XP_006722618.1:n.121+35282A>G
XM_017026033.1:c.121+35282A>G XP_016881522.1:n.121+35282A>G
XM_017026034.1:c.-148+35282A>G XP_016881523.1:n.-148+35282A>G
NM_031422.6:c.121+35282A>G MANE Select NP_113610.2:n.121+35282A>G
NM_001256316.2:c.121+35282A>G NP_001243245.1:n.121+35282A>G
NM_001398493.1:c.121+35282A>G NP_001385422.1:n.121+35282A>G
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