Canonical Allele Identifier: CA9452729
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs753734813
ExAC: 19:41351088 T / A
gnomAD v2: 19-41351088-T-A
gnomAD v4: 19-40845183-T-A
MyVariant Identifiers: chr19:g.41351088T>A (hg19) chr19:g.40845183T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845183T>A , CM000681.2:g.40845183T>A GRCh38
NC_000019.9:g.41351088T>A , CM000681.1:g.41351088T>A GRCh37
NC_000019.8:g.46042928T>A NCBI36
NG_008377.1:g.10265A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1161+111A>T MANE Select ENSP00000301141.4:n.1161+111A>T
ENST00000301141.9:c.1161+111A>T ENSP00000301141.4:n.1161+111A>T
ENST00000596719.5:n.1123A>T
ENST00000601627.1:c.119+43768T>A
ENST00000610301.1:c.1161+111A>T ENSP00000477899.1:n.1161+111A>T
NM_000762.5:c.1161+111A>T NP_000753.3:n.1161+111A>T
NM_000762.6:c.1161+111A>T MANE Select NP_000753.3:n.1161+111A>T
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