Canonical Allele Identifier: CA2585204267
Gene: CYP2A6 HGNC NCBI

Linked Data

gnomAD v4: 19-40845052-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845052T>G , CM000681.2:g.40845052T>G GRCh38
NC_000019.9:g.41350957T>G , CM000681.1:g.41350957T>G GRCh37
NC_000019.8:g.46042797T>G NCBI36
NG_008377.1:g.10396A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1161+242A>C MANE Select ENSP00000301141.4:n.1161+242A>C
ENST00000301141.9:c.1161+242A>C ENSP00000301141.4:n.1161+242A>C
ENST00000596719.5:n.1254A>C
ENST00000601627.1:c.119+43637T>G
ENST00000610301.1:c.1161+242A>C ENSP00000477899.1:n.1161+242A>C
NM_000762.5:c.1161+242A>C NP_000753.3:n.1161+242A>C
NM_000762.6:c.1161+242A>C MANE Select NP_000753.3:n.1161+242A>C
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