Canonical Allele Identifier: CA405965465
Gene: CYP2A6 HGNC NCBI

Linked Data

gnomAD v4: 19-40848331-A-C
MyVariant Identifiers: chr19:g.41354236A>C (hg19) chr19:g.40848331A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848331A>C , CM000681.2:g.40848331A>C GRCh38
NC_000019.9:g.41354236A>C , CM000681.1:g.41354236A>C GRCh37
NC_000019.8:g.46046076A>C NCBI36
NG_008377.1:g.7117T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.542T>G MANE Select ENSP00000301141.4:p.Val181Gly
ENST00000301141.9:c.542T>G ENSP00000301141.4:p.Val181Gly
ENST00000596719.5:n.393T>G
ENST00000600495.1:c.*354T>G ENSP00000472905.1:n.*354T>G
ENST00000601627.1:c.120-43660A>C
ENST00000610301.1:c.542T>G ENSP00000477899.1:p.Val181Gly
NM_000762.5:c.542T>G NP_000753.3:p.Val181Gly
NM_000762.6:c.542T>G MANE Select NP_000753.3:p.Val181Gly
Search 100 bp 5'
Search 100 bp 3'