Canonical Allele Identifier: CA393179165

Gene: CYP1A2

Linked Data

• MyVariant Identifiers: chr15:g.75042607G>T (hg19) ; chr15:g.74750266G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74750266G>T , CM000677.2:g.74750266G>T	GRCh38
NC_000015.9:g.75042607G>T , CM000677.1:g.75042607G>T	GRCh37
NC_000015.8:g.72829660G>T	NCBI36
NG_008431.1:g.32725G>T
NG_008431.2:g.32725G>T
NG_061543.1:g.6422G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.528G>T MANE Select	ENSP00000342007.4:p.Leu176Phe
ENST00000343932.4:c.528G>T	ENSP00000342007.4:p.Leu176Phe
NM_000761.4:c.528G>T	NP_000752.2:p.Leu176Phe
NM_000761.5:c.528G>T MANE Select	NP_000752.2:p.Leu176Phe