Canonical Allele Identifier: CA2187824269

Gene: CYP1A2

Linked Data

• dbSNP Id: rs2063301727

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74749068C>G , CM000677.2:g.74749068C>G	GRCh38
NC_000015.9:g.75041409C>G , CM000677.1:g.75041409C>G	GRCh37
NC_000015.8:g.72828462C>G	NCBI36
NG_008431.1:g.31527C>G
NG_008431.2:g.31527C>G
NG_061543.1:g.5224C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.-10+171C>G MANE Select	ENSP00000342007.4:n.-10+171C>G
ENST00000343932.4:c.-10+171C>G	ENSP00000342007.4:n.-10+171C>G
NM_000761.4:c.-10+171C>G	NP_000752.2:n.-10+171C>G
NM_000761.5:c.-10+171C>G MANE Select	NP_000752.2:n.-10+171C>G