Canonical Allele Identifier: CA9453015
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs56256500
ExAC: 19:41354171 G / A
gnomAD v2: 19-41354171-G-A
gnomAD v3: 19-40848266-G-A
gnomAD v4: 19-40848266-G-A
COSMIC: COSM1393903
MyVariant Identifiers: chr19:g.41354171G>A (hg19) chr19:g.40848266G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848266G>A , CM000681.2:g.40848266G>A GRCh38
NC_000019.9:g.41354171G>A , CM000681.1:g.41354171G>A GRCh37
NC_000019.8:g.46046011G>A NCBI36
NG_008377.1:g.7182C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.607C>T MANE Select ENSP00000301141.4:p.Arg203Cys
ENST00000301141.9:c.607C>T ENSP00000301141.4:p.Arg203Cys
ENST00000596719.5:n.458C>T
ENST00000600495.1:c.*419C>T ENSP00000472905.1:n.*419C>T
ENST00000601627.1:c.120-43725G>A
ENST00000610301.1:c.607C>T ENSP00000477899.1:p.Arg203Cys
NM_000762.5:c.607C>T NP_000753.3:p.Arg203Cys
NM_000762.6:c.607C>T MANE Select NP_000753.3:p.Arg203Cys
Search 100 bp 5'
Search 100 bp 3'