Canonical Allele Identifier: CA491489098

Gene: CYP1A2

Linked Data

• dbSNP Id: rs1162665369
• gnomAD v2: 15-75042310-G-A
• gnomAD v3: 15-74749969-G-A
• gnomAD v4: 15-74749969-G-A
• MyVariant Identifiers: chr15:g.75042310G>A (hg19) ; chr15:g.74749969G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74749969G>A , CM000677.2:g.74749969G>A	GRCh38
NC_000015.9:g.75042310G>A , CM000677.1:g.75042310G>A	GRCh37
NC_000015.8:g.72829363G>A	NCBI36
NG_008431.1:g.32428G>A
NG_008431.2:g.32428G>A
NG_061543.1:g.6125G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.231G>A MANE Select	ENSP00000342007.4:p.Gln77=
ENST00000343932.4:c.231G>A	ENSP00000342007.4:p.Gln77=
NM_000761.4:c.231G>A	NP_000752.2:p.Gln77=
NM_000761.5:c.231G>A MANE Select	NP_000752.2:p.Gln77=