Canonical Allele Identifier: CA2187826221
Gene: CYP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74753134T= , CM000677.2:g.74753134T= GRCh38
NC_000015.9:g.75045475T= , CM000677.1:g.75045475T= GRCh37
NC_000015.8:g.72832528T= NCBI36
NG_008431.1:g.35593T=
NG_008431.2:g.35593T=
NG_061543.1:g.9290T=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1167-50T= MANE Select ENSP00000342007.4:n.1167-50T=
ENST00000343932.4:c.1167-50T= ENSP00000342007.4:n.1167-50T=
NM_000761.4:c.1167-50T= NP_000752.2:n.1167-50T=
NM_000761.5:c.1167-50T= MANE Select NP_000752.2:n.1167-50T=
Search 100 bp 5'
Search 100 bp 3'