Canonical Allele Identifier: CA308456289
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs562603344
gnomAD v3: 19-40848018-G-C
gnomAD v4: 19-40848018-G-C
MyVariant Identifiers: chr19:g.41353923G>C (hg19) chr19:g.40848018G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848018G>C , CM000681.2:g.40848018G>C GRCh38
NC_000019.9:g.41353923G>C , CM000681.1:g.41353923G>C GRCh37
NC_000019.8:g.46045763G>C NCBI36
NG_008377.1:g.7430C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.654+201C>G MANE Select ENSP00000301141.4:n.654+201C>G
ENST00000301141.9:c.654+201C>G ENSP00000301141.4:n.654+201C>G
ENST00000596719.5:n.505+201C>G
ENST00000600495.1:c.*466+201C>G ENSP00000472905.1:n.*466+201C>G
ENST00000601627.1:c.120-43973G>C
ENST00000610301.1:c.654+201C>G ENSP00000477899.1:n.654+201C>G
NM_000762.5:c.654+201C>G NP_000753.3:n.654+201C>G
NM_000762.6:c.654+201C>G MANE Select NP_000753.3:n.654+201C>G
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