Canonical Allele Identifier: CA7660072
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs144148965

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754843G>A , CM000677.2:g.74754843G>A GRCh38
NC_000015.9:g.75047184G>A , CM000677.1:g.75047184G>A GRCh37
NC_000015.8:g.72834237G>A NCBI36
NG_008431.1:g.37302G>A
NG_008431.2:g.37302G>A
NG_061543.1:g.10999G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1306G>A MANE Select ENSP00000342007.4:p.Asp436Asn
ENST00000343932.4:c.1306G>A ENSP00000342007.4:p.Asp436Asn
NM_000761.4:c.1306G>A NP_000752.2:p.Asp436Asn
NM_000761.5:c.1306G>A MANE Select NP_000752.2:p.Asp436Asn