Canonical Allele Identifier: CA9452759
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs759381042
ExAC: 19:41351183 TG / T
gnomAD v2: 19-41351183-TG-T
gnomAD v3: 19-40845278-TG-T
gnomAD v4: 19-40845278-TG-T
MyVariant Identifiers: chr19:g.41351184del (hg19) chr19:g.40845279del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845283del , CM000681.2:g.40845283del GRCh38
NC_000019.9:g.41351188del , CM000681.1:g.41351188del GRCh37
NC_000019.8:g.46043028del NCBI36
NG_008377.1:g.10169del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1161+15del MANE Select ENSP00000301141.4:n.1161+15del
ENST00000301141.9:c.1161+15del ENSP00000301141.4:n.1161+15del
ENST00000596719.5:n.1027del
ENST00000601627.1:c.119+43868del
ENST00000610301.1:c.1161+15del ENSP00000477899.1:n.1161+15del
NM_000762.5:c.1161+15del NP_000753.3:n.1161+15del
NM_000762.6:c.1161+15del MANE Select NP_000753.3:n.1161+15del
Search 100 bp 5'
Search 100 bp 3'