Canonical Allele Identifier: CA633468371
Gene: CYP2A6 HGNC NCBI

Linked Data

dbSNP Id: rs1279399910
gnomAD v2: 19-41351030-AG-A
gnomAD v4: 19-40845125-AG-A
MyVariant Identifiers: chr19:g.41351031del (hg19) chr19:g.40845126del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.40845127del , CM000681.2:g.40845127del GRCh38
NC_000019.9:g.41351032del , CM000681.1:g.41351032del GRCh37
NC_000019.8:g.46042872del NCBI36
NG_008377.1:g.10322del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301141.10:c.1161+168del MANE Select ENSP00000301141.4:n.1161+168del
ENST00000301141.9:c.1161+168del ENSP00000301141.4:n.1161+168del
ENST00000596719.5:n.1180del
ENST00000601627.1:c.119+43712del
ENST00000610301.1:c.1161+168del ENSP00000477899.1:n.1161+168del
NM_000762.5:c.1161+168del NP_000753.3:n.1161+168del
NM_000762.6:c.1161+168del MANE Select NP_000753.3:n.1161+168del
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Search 100 bp 3'