Canonical Allele Identifier: CA7659961

Gene: CYP1A2

Linked Data

• dbSNP Id: rs529731621
• ExAC: 15:75044423 T / C
• gnomAD v2: 15-75044423-T-C
• gnomAD v3: 15-74752082-T-C
• gnomAD v4: 15-74752082-T-C
• MyVariant Identifiers: chr15:g.75044423T>C (hg19) ; chr15:g.74752082T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74752082T>C , CM000677.2:g.74752082T>C	GRCh38
NC_000015.9:g.75044423T>C , CM000677.1:g.75044423T>C	GRCh37
NC_000015.8:g.72831476T>C	NCBI36
NG_008431.1:g.34541T>C
NG_008431.2:g.34541T>C
NG_061543.1:g.8238T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000343932.5:c.1043-42T>C MANE Select	ENSP00000342007.4:n.1043-42T>C
ENST00000343932.4:c.1043-42T>C	ENSP00000342007.4:n.1043-42T>C
NM_000761.4:c.1043-42T>C	NP_000752.2:n.1043-42T>C
NM_000761.5:c.1043-42T>C MANE Select	NP_000752.2:n.1043-42T>C