Canonical Allele Identifier: CA272815231
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs988250207

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74752060_74752061del , CM000677.2:g.74752060_74752061del GRCh38
NC_000015.9:g.75044401_75044402del , CM000677.1:g.75044401_75044402del GRCh37
NC_000015.8:g.72831454_72831455del NCBI36
NG_008431.1:g.34519_34520del
NG_008431.2:g.34519_34520del
NG_061543.1:g.8216_8217del

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1043-64_1043-63del MANE Select ENSP00000342007.4:n.1043-64_1043-63del
ENST00000343932.4:c.1043-64_1043-63del ENSP00000342007.4:n.1043-64_1043-63del
NM_000761.4:c.1043-64_1043-63del NP_000752.2:n.1043-64_1043-63del
NM_000761.5:c.1043-64_1043-63del MANE Select NP_000752.2:n.1043-64_1043-63del