Canonical Allele Identifier: CA619121377
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1310480530

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749557A>C , CM000677.2:g.74749557A>C GRCh38
NC_000015.9:g.75041898A>C , CM000677.1:g.75041898A>C GRCh37
NC_000015.8:g.72828951A>C NCBI36
NG_008431.1:g.32016A>C
NG_008431.2:g.32016A>C
NG_061543.1:g.5713A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-173A>C MANE Select ENSP00000342007.4:n.-9-173A>C
ENST00000343932.4:c.-9-173A>C ENSP00000342007.4:n.-9-173A>C
NM_000761.4:c.-9-173A>C NP_000752.2:n.-9-173A>C
NM_000761.5:c.-9-173A>C MANE Select NP_000752.2:n.-9-173A>C