Canonical Allele Identifier: CA2629512116

Gene: CYP1A2

Linked Data

• gnomAD v4: 15-74755294-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755294G>T , CM000677.2:g.74755294G>T	GRCh38
NC_000015.9:g.75047635G>T , CM000677.1:g.75047635G>T	GRCh37
NC_000015.8:g.72834688G>T	NCBI36
NG_008431.1:g.37753G>T
NG_008431.2:g.37753G>T
NG_061543.1:g.11450G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*206G>T MANE Select	ENSP00000342007.4:n.*206G>T
ENST00000343932.4:c.*206G>T	ENSP00000342007.4:n.*206G>T
NM_000761.4:c.*206G>T	NP_000752.2:n.*206G>T
NM_000761.5:c.*206G>T MANE Select	NP_000752.2:n.*206G>T