Canonical Allele Identifier: CA393179248
Gene: CYP1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.75042635T>A (hg19) chr15:g.74750294T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74750294T>A , CM000677.2:g.74750294T>A GRCh38
NC_000015.9:g.75042635T>A , CM000677.1:g.75042635T>A GRCh37
NC_000015.8:g.72829688T>A NCBI36
NG_008431.1:g.32753T>A
NG_008431.2:g.32753T>A
NG_061543.1:g.6450T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.556T>A MANE Select ENSP00000342007.4:p.Phe186Ile
ENST00000343932.4:c.556T>A ENSP00000342007.4:p.Phe186Ile
NM_000761.4:c.556T>A NP_000752.2:p.Phe186Ile
NM_000761.5:c.556T>A MANE Select NP_000752.2:p.Phe186Ile
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