Canonical Allele Identifier: CA715671010
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1367910185

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755016del , CM000677.2:g.74755016del GRCh38
NC_000015.9:g.75047357del , CM000677.1:g.75047357del GRCh37
NC_000015.8:g.72834410del NCBI36
NG_008431.1:g.37475del
NG_008431.2:g.37475del
NG_061543.1:g.11172del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1479del MANE Select ENSP00000342007.4:p.Ile494SerfsTer4
ENST00000343932.4:c.1479del ENSP00000342007.4:p.Ile494SerfsTer4
NM_000761.4:c.1479del NP_000752.2:p.Ile494SerfsTer4
NM_000761.5:c.1479del MANE Select NP_000752.2:p.Ile494SerfsTer4