Canonical Allele Identifier: CA491489206

Gene: CYP1A2

Linked Data

• COSMIC: COSM964888
• MyVariant Identifiers: chr15:g.75042139C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74749798C>T , CM000677.2:g.74749798C>T	GRCh38
NC_000015.9:g.75042139C>T , CM000677.1:g.75042139C>T	GRCh37
NC_000015.8:g.72829192C>T	NCBI36
NG_008431.1:g.32257C>T
NG_008431.2:g.32257C>T
NG_061543.1:g.5954C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.60C>T MANE Select	ENSP00000342007.4:p.Ile20=
ENST00000343932.4:c.60C>T	ENSP00000342007.4:p.Ile20=
NM_000761.4:c.60C>T	NP_000752.2:p.Ile20=
NM_000761.5:c.60C>T MANE Select	NP_000752.2:p.Ile20=