Canonical Allele Identifier: CA405965625
Gene: CYP2A6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.41354545A>C (hg19) chr19:g.40848640A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848640A>C , CM000681.2:g.40848640A>C GRCh38
NC_000019.9:g.41354545A>C , CM000681.1:g.41354545A>C GRCh37
NC_000019.8:g.46046385A>C NCBI36
NG_008377.1:g.6808T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.467T>G MANE Select ENSP00000301141.4:p.Leu156Arg
ENST00000301141.9:c.467T>G ENSP00000301141.4:p.Leu156Arg
ENST00000596719.5:n.318T>G
ENST00000600495.1:c.*279T>G ENSP00000472905.1:n.*279T>G
ENST00000601627.1:c.120-43351A>C
ENST00000610301.1:c.467T>G ENSP00000477899.1:p.Leu156Arg
NM_000762.5:c.467T>G NP_000753.3:p.Leu156Arg
NM_000762.6:c.467T>G MANE Select NP_000753.3:p.Leu156Arg
Search 100 bp 5'
Search 100 bp 3'