Canonical Allele Identifier: CA2585205041
Gene: CYP2A6 HGNC NCBI

Linked Data

gnomAD v4: 19-40848450-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848450A>T , CM000681.2:g.40848450A>T GRCh38
NC_000019.9:g.41354355A>T , CM000681.1:g.41354355A>T GRCh37
NC_000019.8:g.46046195A>T NCBI36
NG_008377.1:g.6998T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.494-71T>A MANE Select ENSP00000301141.4:n.494-71T>A
ENST00000301141.9:c.494-71T>A ENSP00000301141.4:n.494-71T>A
ENST00000596719.5:n.345-71T>A
ENST00000600495.1:c.*306-71T>A ENSP00000472905.1:n.*306-71T>A
ENST00000601627.1:c.120-43541A>T
ENST00000610301.1:c.494-71T>A ENSP00000477899.1:n.494-71T>A
NM_000762.5:c.494-71T>A NP_000753.3:n.494-71T>A
NM_000762.6:c.494-71T>A MANE Select NP_000753.3:n.494-71T>A
Search 100 bp 5'
Search 100 bp 3'