Canonical Allele Identifier: CA405965619
Gene: CYP2A6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.41354542A>T (hg19) chr19:g.40848637A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848637A>T , CM000681.2:g.40848637A>T GRCh38
NC_000019.9:g.41354542A>T , CM000681.1:g.41354542A>T GRCh37
NC_000019.8:g.46046382A>T NCBI36
NG_008377.1:g.6811T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.470T>A MANE Select ENSP00000301141.4:p.Ile157Asn
ENST00000301141.9:c.470T>A ENSP00000301141.4:p.Ile157Asn
ENST00000596719.5:n.321T>A
ENST00000600495.1:c.*282T>A ENSP00000472905.1:n.*282T>A
ENST00000601627.1:c.120-43354A>T
ENST00000610301.1:c.470T>A ENSP00000477899.1:p.Ile157Asn
NM_000762.5:c.470T>A NP_000753.3:p.Ile157Asn
NM_000762.6:c.470T>A MANE Select NP_000753.3:p.Ile157Asn
Search 100 bp 5'
Search 100 bp 3'