Canonical Allele Identifier: CA308456642
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs951987757
gnomAD v2: 19-41354386-A-G
gnomAD v3: 19-40848481-A-G
gnomAD v4: 19-40848481-A-G
MyVariant Identifiers: chr19:g.41354386A>G (hg19) chr19:g.40848481A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848481A>G , CM000681.2:g.40848481A>G GRCh38
NC_000019.9:g.41354386A>G , CM000681.1:g.41354386A>G GRCh37
NC_000019.8:g.46046226A>G NCBI36
NG_008377.1:g.6967T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000301141.10:c.494-102T>C MANE Select ENSP00000301141.4:n.494-102T>C
ENST00000301141.9:c.494-102T>C ENSP00000301141.4:n.494-102T>C
ENST00000596719.5:n.345-102T>C
ENST00000600495.1:c.*306-102T>C ENSP00000472905.1:n.*306-102T>C
ENST00000601627.1:c.120-43510A>G
ENST00000610301.1:c.494-102T>C ENSP00000477899.1:n.494-102T>C
NM_000762.5:c.494-102T>C NP_000753.3:n.494-102T>C
NM_000762.6:c.494-102T>C MANE Select NP_000753.3:n.494-102T>C
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