Canonical Allele Identifier: CA9453092
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs60563539
ExAC: 19:41354534 G / T
gnomAD v2: 19-41354534-G-T
gnomAD v3: 19-40848629-G-T
gnomAD v4: 19-40848629-G-T
MyVariant Identifiers: chr19:g.41354534G>T (hg19) chr19:g.40848629G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848629G>T , CM000681.2:g.40848629G>T GRCh38
NC_000019.9:g.41354534G>T , CM000681.1:g.41354534G>T GRCh37
NC_000019.8:g.46046374G>T NCBI36
NG_008377.1:g.6819C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.478C>A MANE Select ENSP00000301141.4:p.Leu160Ile
ENST00000301141.9:c.478C>A ENSP00000301141.4:p.Leu160Ile
ENST00000596719.5:n.329C>A
ENST00000600495.1:c.*290C>A ENSP00000472905.1:n.*290C>A
ENST00000601627.1:c.120-43362G>T
ENST00000610301.1:c.478C>A ENSP00000477899.1:p.Leu160Ile
NM_000762.5:c.478C>A NP_000753.3:p.Leu160Ile
NM_000762.6:c.478C>A MANE Select NP_000753.3:p.Leu160Ile
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Search 100 bp 3'