Canonical Allele Identifier: CA491219694

Gene: CYP1A2

Linked Data

• dbSNP Id: rs1308458059
• gnomAD v2: 15-75044481-G-A
• gnomAD v3: 15-74752140-G-A
• gnomAD v4: 15-74752140-G-A
• MyVariant Identifiers: chr15:g.75044481G>A (hg19) ; chr15:g.74752140G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74752140G>A , CM000677.2:g.74752140G>A	GRCh38
NC_000015.9:g.75044481G>A , CM000677.1:g.75044481G>A	GRCh37
NC_000015.8:g.72831534G>A	NCBI36
NG_008431.1:g.34599G>A
NG_008431.2:g.34599G>A
NG_061543.1:g.8296G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.1059G>A MANE Select	ENSP00000342007.4:p.Arg353=
ENST00000343932.4:c.1059G>A	ENSP00000342007.4:p.Arg353=
NM_000761.4:c.1059G>A	NP_000752.2:p.Arg353=
NM_000761.5:c.1059G>A MANE Select	NP_000752.2:p.Arg353=