Canonical Allele Identifier: CA393169749

Gene: CYP1A2

Linked Data

• MyVariant Identifiers: chr15:g.75047261A>T (hg19) ; chr15:g.74754920A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74754920A>T , CM000677.2:g.74754920A>T	GRCh38
NC_000015.9:g.75047261A>T , CM000677.1:g.75047261A>T	GRCh37
NC_000015.8:g.72834314A>T	NCBI36
NG_008431.1:g.37379A>T
NG_008431.2:g.37379A>T
NG_061543.1:g.11076A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.1383A>T MANE Select	ENSP00000342007.4:p.Glu461Asp
ENST00000343932.4:c.1383A>T	ENSP00000342007.4:p.Glu461Asp
NM_000761.4:c.1383A>T	NP_000752.2:p.Glu461Asp
NM_000761.5:c.1383A>T MANE Select	NP_000752.2:p.Glu461Asp