Canonical Allele Identifier: CA633468381
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs1235280500
gnomAD v2: 19-41351083-T-C
gnomAD v4: 19-40845178-T-C
MyVariant Identifiers: chr19:g.41351083T>C (hg19) chr19:g.40845178T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845178T>C , CM000681.2:g.40845178T>C GRCh38
NC_000019.9:g.41351083T>C , CM000681.1:g.41351083T>C GRCh37
NC_000019.8:g.46042923T>C NCBI36
NG_008377.1:g.10270A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1161+116A>G MANE Select ENSP00000301141.4:n.1161+116A>G
ENST00000301141.9:c.1161+116A>G ENSP00000301141.4:n.1161+116A>G
ENST00000596719.5:n.1128A>G
ENST00000601627.1:c.119+43763T>C
ENST00000610301.1:c.1161+116A>G ENSP00000477899.1:n.1161+116A>G
NM_000762.5:c.1161+116A>G NP_000753.3:n.1161+116A>G
NM_000762.6:c.1161+116A>G MANE Select NP_000753.3:n.1161+116A>G
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