Canonical Allele Identifier: CA2629509301
Gene: CYP1A2 HGNC NCBI

Linked Data

gnomAD v4: 15-74751895-GA-G
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751896del , CM000677.2:g.74751896del GRCh38
NC_000015.9:g.75044237del , CM000677.1:g.75044237del GRCh37
NC_000015.8:g.72831290del NCBI36
NG_008431.1:g.34355del
NG_008431.2:g.34355del
NG_061543.1:g.8052del

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1042+42del MANE Select ENSP00000342007.4:n.1042+42del
ENST00000343932.4:c.1042+42del ENSP00000342007.4:n.1042+42del
NM_000761.4:c.1042+42del NP_000752.2:n.1042+42del
NM_000761.5:c.1042+42del MANE Select NP_000752.2:n.1042+42del
Search 100 bp 5'
Search 100 bp 3'