Canonical Allele Identifier: CA393169569

Gene: CYP1A2

Linked Data

• MyVariant Identifiers: chr15:g.75047227T>A (hg19) ; chr15:g.74754886T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74754886T>A , CM000677.2:g.74754886T>A	GRCh38
NC_000015.9:g.75047227T>A , CM000677.1:g.75047227T>A	GRCh37
NC_000015.8:g.72834280T>A	NCBI36
NG_008431.1:g.37345T>A
NG_008431.2:g.37345T>A
NG_061543.1:g.11042T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.1349T>A MANE Select	ENSP00000342007.4:p.Leu450Gln
ENST00000343932.4:c.1349T>A	ENSP00000342007.4:p.Leu450Gln
NM_000761.4:c.1349T>A	NP_000752.2:p.Leu450Gln
NM_000761.5:c.1349T>A MANE Select	NP_000752.2:p.Leu450Gln