Canonical Allele Identifier: CA7660075
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs45486893

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754850C>T , CM000677.2:g.74754850C>T GRCh38
NC_000015.9:g.75047191C>T , CM000677.1:g.75047191C>T GRCh37
NC_000015.8:g.72834244C>T NCBI36
NG_008431.1:g.37309C>T
NG_008431.2:g.37309C>T
NG_061543.1:g.11006C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1313C>T MANE Select ENSP00000342007.4:p.Thr438Ile
ENST00000343932.4:c.1313C>T ENSP00000342007.4:p.Thr438Ile
NM_000761.4:c.1313C>T NP_000752.2:p.Thr438Ile
NM_000761.5:c.1313C>T MANE Select NP_000752.2:p.Thr438Ile