Canonical Allele Identifier: CA9452762
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs774691324
ExAC: 19:41351188 G / T
gnomAD v2: 19-41351188-G-T
gnomAD v3: 19-40845283-G-T
gnomAD v4: 19-40845283-G-T
MyVariant Identifiers: chr19:g.41351188G>T (hg19) chr19:g.40845283G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845283G>T , CM000681.2:g.40845283G>T GRCh38
NC_000019.9:g.41351188G>T , CM000681.1:g.41351188G>T GRCh37
NC_000019.8:g.46043028G>T NCBI36
NG_008377.1:g.10165C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1161+11C>A MANE Select ENSP00000301141.4:n.1161+11C>A
ENST00000301141.9:c.1161+11C>A ENSP00000301141.4:n.1161+11C>A
ENST00000596719.5:n.1023C>A
ENST00000601627.1:c.119+43868G>T
ENST00000610301.1:c.1161+11C>A ENSP00000477899.1:n.1161+11C>A
NM_000762.5:c.1161+11C>A NP_000753.3:n.1161+11C>A
NM_000762.6:c.1161+11C>A MANE Select NP_000753.3:n.1161+11C>A
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