Canonical Allele Identifier: CA971498327
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs2063304351
gnomAD v3: 15-74749666-G-A
gnomAD v4: 15-74749666-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749666G>A , CM000677.2:g.74749666G>A GRCh38
NC_000015.9:g.75042007G>A , CM000677.1:g.75042007G>A GRCh37
NC_000015.8:g.72829060G>A NCBI36
NG_008431.1:g.32125G>A
NG_008431.2:g.32125G>A
NG_061543.1:g.5822G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-64G>A MANE Select ENSP00000342007.4:n.-9-64G>A
ENST00000343932.4:c.-9-64G>A ENSP00000342007.4:n.-9-64G>A
NM_000761.4:c.-9-64G>A NP_000752.2:n.-9-64G>A
NM_000761.5:c.-9-64G>A MANE Select NP_000752.2:n.-9-64G>A
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