Canonical Allele Identifier: CA2629504969
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74754677-T-TTGCTTTCAAAGTGCCCTCACACTTGTG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754679_74754705dup , CM000677.2:g.74754679_74754705dup GRCh38
NC_000015.9:g.75047020_75047046dup , CM000677.1:g.75047020_75047046dup GRCh37
NC_000015.8:g.72834073_72834099dup NCBI36
NG_008431.1:g.37138_37164dup
NG_008431.2:g.37138_37164dup
NG_061543.1:g.10835_10861dup

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1254-112_1254-86dup MANE Select ENSP00000342007.4:n.1254-112_1254-86dup
ENST00000343932.4:c.1254-112_1254-86dup ENSP00000342007.4:n.1254-112_1254-86dup
NM_000761.4:c.1254-112_1254-86dup NP_000752.2:n.1254-112_1254-86dup
NM_000761.5:c.1254-112_1254-86dup MANE Select NP_000752.2:n.1254-112_1254-86dup
Search 100 bp 5'
Search 100 bp 3'