Canonical Allele Identifier: CA507688185
Gene: CYP2A6 HGNC NCBI

Linked Data

gnomAD v4: 19-40848630-G-A
MyVariant Identifiers: chr19:g.41354535G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848630G>A , CM000681.2:g.40848630G>A GRCh38
NC_000019.9:g.41354535G>A , CM000681.1:g.41354535G>A GRCh37
NC_000019.8:g.46046375G>A NCBI36
NG_008377.1:g.6818C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.477C>T MANE Select ENSP00000301141.4:p.Ala159=
ENST00000301141.9:c.477C>T ENSP00000301141.4:p.Ala159=
ENST00000596719.5:n.328C>T
ENST00000600495.1:c.*289C>T ENSP00000472905.1:n.*289C>T
ENST00000601627.1:c.120-43361G>A
ENST00000610301.1:c.477C>T ENSP00000477899.1:p.Ala159=
NM_000762.5:c.477C>T NP_000753.3:p.Ala159=
NM_000762.6:c.477C>T MANE Select NP_000753.3:p.Ala159=
Search 100 bp 5'
Search 100 bp 3'