Canonical Allele Identifier: CA507688246
Gene: CYP2A6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.41354169G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848264G>A , CM000681.2:g.40848264G>A GRCh38
NC_000019.9:g.41354169G>A , CM000681.1:g.41354169G>A GRCh37
NC_000019.8:g.46046009G>A NCBI36
NG_008377.1:g.7184C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.609C>T MANE Select ENSP00000301141.4:p.Arg203=
ENST00000301141.9:c.609C>T ENSP00000301141.4:p.Arg203=
ENST00000596719.5:n.460C>T
ENST00000600495.1:c.*421C>T ENSP00000472905.1:n.*421C>T
ENST00000601627.1:c.120-43727G>A
ENST00000610301.1:c.609C>T ENSP00000477899.1:p.Arg203=
NM_000762.5:c.609C>T NP_000753.3:p.Arg203=
NM_000762.6:c.609C>T MANE Select NP_000753.3:p.Arg203=