Canonical Allele Identifier: CA882277072
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs1471555495
gnomAD v3: 19-40845026-A-G
gnomAD v4: 19-40845026-A-G
MyVariant Identifiers: chr19:g.41350931A>G (hg19) chr19:g.40845026A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845026A>G , CM000681.2:g.40845026A>G GRCh38
NC_000019.9:g.41350931A>G , CM000681.1:g.41350931A>G GRCh37
NC_000019.8:g.46042771A>G NCBI36
NG_008377.1:g.10422T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1162-254T>C MANE Select ENSP00000301141.4:n.1162-254T>C
ENST00000301141.9:c.1162-254T>C ENSP00000301141.4:n.1162-254T>C
ENST00000596719.5:n.1280T>C
ENST00000601627.1:c.119+43611A>G
ENST00000610301.1:c.1162-254T>C ENSP00000477899.1:n.1162-254T>C
NM_000762.5:c.1162-254T>C NP_000753.3:n.1162-254T>C
NM_000762.6:c.1162-254T>C MANE Select NP_000753.3:n.1162-254T>C
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