Canonical Allele Identifier: CA507688325

Gene: CYP2A6

Linked Data

• MyVariant Identifiers: chr19:g.41351271T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40845366T>G , CM000681.2:g.40845366T>G	GRCh38
NC_000019.9:g.41351271T>G , CM000681.1:g.41351271T>G	GRCh37
NC_000019.8:g.46043111T>G	NCBI36
NG_008377.1:g.10082A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301141.10:c.1089A>C MANE Select	ENSP00000301141.4:p.Gly363=
ENST00000301141.9:c.1089A>C	ENSP00000301141.4:p.Gly363=
ENST00000596719.5:n.940A>C
ENST00000601627.1:c.119+43951T>G
ENST00000610301.1:c.1089A>C	ENSP00000477899.1:p.Gly363=
NM_000762.5:c.1089A>C	NP_000753.3:p.Gly363=
NM_000762.6:c.1089A>C MANE Select	NP_000753.3:p.Gly363=