Canonical Allele Identifier: CA715671330
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1446027009
gnomAD v3: 15-74755363-A-G
gnomAD v4: 15-74755363-A-G
MyVariant Identifiers: chr15:g.75047704A>G (hg19) chr15:g.74755363A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755363A>G , CM000677.2:g.74755363A>G GRCh38
NC_000015.9:g.75047704A>G , CM000677.1:g.75047704A>G GRCh37
NC_000015.8:g.72834757A>G NCBI36
NG_008431.1:g.37822A>G
NG_008431.2:g.37822A>G
NG_061543.1:g.11519A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*275A>G MANE Select ENSP00000342007.4:n.*275A>G
ENST00000343932.4:c.*275A>G ENSP00000342007.4:n.*275A>G
NM_000761.4:c.*275A>G NP_000752.2:n.*275A>G
NM_000761.5:c.*275A>G MANE Select NP_000752.2:n.*275A>G
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