Canonical Allele Identifier: CA405965607
Gene: CYP2A6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.41354536G>T (hg19) chr19:g.40848631G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848631G>T , CM000681.2:g.40848631G>T GRCh38
NC_000019.9:g.41354536G>T , CM000681.1:g.41354536G>T GRCh37
NC_000019.8:g.46046376G>T NCBI36
NG_008377.1:g.6817C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.476C>A MANE Select ENSP00000301141.4:p.Ala159Asp
ENST00000301141.9:c.476C>A ENSP00000301141.4:p.Ala159Asp
ENST00000596719.5:n.327C>A
ENST00000600495.1:c.*288C>A ENSP00000472905.1:n.*288C>A
ENST00000601627.1:c.120-43360G>T
ENST00000610301.1:c.476C>A ENSP00000477899.1:p.Ala159Asp
NM_000762.5:c.476C>A NP_000753.3:p.Ala159Asp
NM_000762.6:c.476C>A MANE Select NP_000753.3:p.Ala159Asp
Search 100 bp 5'
Search 100 bp 3'