Canonical Allele Identifier: CA507688228
Gene: CYP2A6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.41354139T>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848234T>G , CM000681.2:g.40848234T>G GRCh38
NC_000019.9:g.41354139T>G , CM000681.1:g.41354139T>G GRCh37
NC_000019.8:g.46045979T>G NCBI36
NG_008377.1:g.7214A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.639A>C MANE Select ENSP00000301141.4:p.Ser213=
ENST00000301141.9:c.639A>C ENSP00000301141.4:p.Ser213=
ENST00000596719.5:n.490A>C
ENST00000600495.1:c.*451A>C ENSP00000472905.1:n.*451A>C
ENST00000601627.1:c.120-43757T>G
ENST00000610301.1:c.639A>C ENSP00000477899.1:p.Ser213=
NM_000762.5:c.639A>C NP_000753.3:p.Ser213=
NM_000762.6:c.639A>C MANE Select NP_000753.3:p.Ser213=
Search 100 bp 5'
Search 100 bp 3'