Canonical Allele Identifier: CA9453019
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs778827400
ExAC: 19:41354175 C / A
gnomAD v2: 19-41354175-C-A
gnomAD v4: 19-40848270-C-A
MyVariant Identifiers: chr19:g.41354175C>A (hg19) chr19:g.40848270C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40848270C>A , CM000681.2:g.40848270C>A GRCh38
NC_000019.9:g.41354175C>A , CM000681.1:g.41354175C>A GRCh37
NC_000019.8:g.46046015C>A NCBI36
NG_008377.1:g.7178G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.603G>T MANE Select ENSP00000301141.4:p.Leu201=
ENST00000301141.9:c.603G>T ENSP00000301141.4:p.Leu201=
ENST00000596719.5:n.454G>T
ENST00000600495.1:c.*415G>T ENSP00000472905.1:n.*415G>T
ENST00000601627.1:c.120-43721C>A
ENST00000610301.1:c.603G>T ENSP00000477899.1:p.Leu201=
NM_000762.5:c.603G>T NP_000753.3:p.Leu201=
NM_000762.6:c.603G>T MANE Select NP_000753.3:p.Leu201=
Search 100 bp 5'
Search 100 bp 3'