Canonical Allele Identifier: CA2585204318
Gene: CYP2A6 HGNC NCBI

Linked Data

gnomAD v4: 19-40845096-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845096C>T , CM000681.2:g.40845096C>T GRCh38
NC_000019.9:g.41351001C>T , CM000681.1:g.41351001C>T GRCh37
NC_000019.8:g.46042841C>T NCBI36
NG_008377.1:g.10352G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1161+198G>A MANE Select ENSP00000301141.4:n.1161+198G>A
ENST00000301141.9:c.1161+198G>A ENSP00000301141.4:n.1161+198G>A
ENST00000596719.5:n.1210G>A
ENST00000601627.1:c.119+43681C>T
ENST00000610301.1:c.1161+198G>A ENSP00000477899.1:n.1161+198G>A
NM_000762.5:c.1161+198G>A NP_000753.3:n.1161+198G>A
NM_000762.6:c.1161+198G>A MANE Select NP_000753.3:n.1161+198G>A
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