Canonical Allele Identifier: CA507688061
Gene: CYP2A6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.41351252A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845347A>G , CM000681.2:g.40845347A>G GRCh38
NC_000019.9:g.41351252A>G , CM000681.1:g.41351252A>G GRCh37
NC_000019.8:g.46043092A>G NCBI36
NG_008377.1:g.10101T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1108T>C MANE Select ENSP00000301141.4:p.Leu370=
ENST00000301141.9:c.1108T>C ENSP00000301141.4:p.Leu370=
ENST00000596719.5:n.959T>C
ENST00000601627.1:c.119+43932A>G
ENST00000610301.1:c.1108T>C ENSP00000477899.1:p.Leu370=
NM_000762.5:c.1108T>C NP_000753.3:p.Leu370=
NM_000762.6:c.1108T>C MANE Select NP_000753.3:p.Leu370=