Canonical Allele Identifier: CA715672206
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1358023450

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749494G>A , CM000677.2:g.74749494G>A GRCh38
NC_000015.9:g.75041835G>A , CM000677.1:g.75041835G>A GRCh37
NC_000015.8:g.72828888G>A NCBI36
NG_008431.1:g.31953G>A
NG_008431.2:g.31953G>A
NG_061543.1:g.5650G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-236G>A MANE Select ENSP00000342007.4:n.-9-236G>A
ENST00000343932.4:c.-9-236G>A ENSP00000342007.4:n.-9-236G>A
NM_000761.4:c.-9-236G>A NP_000752.2:n.-9-236G>A
NM_000761.5:c.-9-236G>A MANE Select NP_000752.2:n.-9-236G>A