Canonical Allele Identifier: CA619122974

Gene: CYP1A2

Linked Data

• dbSNP Id: rs1232045231
• gnomAD v2: 15-75046880-T-G
• gnomAD v3: 15-74754539-T-G
• gnomAD v4: 15-74754539-T-G
• MyVariant Identifiers: chr15:g.75046880T>G (hg19) ; chr15:g.74754539T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74754539T>G , CM000677.2:g.74754539T>G	GRCh38
NC_000015.9:g.75046880T>G , CM000677.1:g.75046880T>G	GRCh37
NC_000015.8:g.72833933T>G	NCBI36
NG_008431.1:g.36998T>G
NG_008431.2:g.36998T>G
NG_061543.1:g.10695T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.1254-252T>G MANE Select	ENSP00000342007.4:n.1254-252T>G
ENST00000343932.4:c.1254-252T>G	ENSP00000342007.4:n.1254-252T>G
NM_000761.4:c.1254-252T>G	NP_000752.2:n.1254-252T>G
NM_000761.5:c.1254-252T>G MANE Select	NP_000752.2:n.1254-252T>G