Canonical Allele Identifier: CA995924042
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs2083448656
gnomAD v3: 19-40845028-G-A
gnomAD v4: 19-40845028-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845028G>A , CM000681.2:g.40845028G>A GRCh38
NC_000019.9:g.41350933G>A , CM000681.1:g.41350933G>A GRCh37
NC_000019.8:g.46042773G>A NCBI36
NG_008377.1:g.10420C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1162-256C>T MANE Select ENSP00000301141.4:n.1162-256C>T
ENST00000301141.9:c.1162-256C>T ENSP00000301141.4:n.1162-256C>T
ENST00000596719.5:n.1278C>T
ENST00000601627.1:c.119+43613G>A
ENST00000610301.1:c.1162-256C>T ENSP00000477899.1:n.1162-256C>T
NM_000762.5:c.1162-256C>T NP_000753.3:n.1162-256C>T
NM_000762.6:c.1162-256C>T MANE Select NP_000753.3:n.1162-256C>T
Search 100 bp 5'
Search 100 bp 3'