Canonical Allele Identifier: CA971499169
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs2082669947

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74752059dup , CM000677.2:g.74752059dup GRCh38
NC_000015.9:g.75044400dup , CM000677.1:g.75044400dup GRCh37
NC_000015.8:g.72831453dup NCBI36
NG_008431.1:g.34518dup
NG_008431.2:g.34518dup
NG_061543.1:g.8215dup

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1043-65dup MANE Select ENSP00000342007.4:n.1043-65dup
ENST00000343932.4:c.1043-65dup ENSP00000342007.4:n.1043-65dup
NM_000761.4:c.1043-65dup NP_000752.2:n.1043-65dup
NM_000761.5:c.1043-65dup MANE Select NP_000752.2:n.1043-65dup