Canonical Allele Identifier: CA507688016
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs1209377065
gnomAD v2: 19-41351223-C-T
gnomAD v4: 19-40845318-C-T
MyVariant Identifiers: chr19:g.41351223C>T (hg19) chr19:g.40845318C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845318C>T , CM000681.2:g.40845318C>T GRCh38
NC_000019.9:g.41351223C>T , CM000681.1:g.41351223C>T GRCh37
NC_000019.8:g.46043063C>T NCBI36
NG_008377.1:g.10130G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1137G>A MANE Select ENSP00000301141.4:p.Lys379=
ENST00000301141.9:c.1137G>A ENSP00000301141.4:p.Lys379=
ENST00000596719.5:n.988G>A
ENST00000601627.1:c.119+43903C>T
ENST00000610301.1:c.1137G>A ENSP00000477899.1:p.Lys379=
NM_000762.5:c.1137G>A NP_000753.3:p.Lys379=
NM_000762.6:c.1137G>A MANE Select NP_000753.3:p.Lys379=
Search 100 bp 5'
Search 100 bp 3'