Canonical Allele Identifier: CA405965460
Gene: CYP2A6 HGNC NCBI

Linked Data

gnomAD v4: 19-40848328-A-C
MyVariant Identifiers: chr19:g.41354233A>C (hg19) chr19:g.40848328A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848328A>C , CM000681.2:g.40848328A>C GRCh38
NC_000019.9:g.41354233A>C , CM000681.1:g.41354233A>C GRCh37
NC_000019.8:g.46046073A>C NCBI36
NG_008377.1:g.7120T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.545T>G MANE Select ENSP00000301141.4:p.Ile182Ser
ENST00000301141.9:c.545T>G ENSP00000301141.4:p.Ile182Ser
ENST00000596719.5:n.396T>G
ENST00000600495.1:c.*357T>G ENSP00000472905.1:n.*357T>G
ENST00000601627.1:c.120-43663A>C
ENST00000610301.1:c.545T>G ENSP00000477899.1:p.Ile182Ser
NM_000762.5:c.545T>G NP_000753.3:p.Ile182Ser
NM_000762.6:c.545T>G MANE Select NP_000753.3:p.Ile182Ser
Search 100 bp 5'
Search 100 bp 3'