Canonical Allele Identifier: CA2187826222
Gene: CYP1A2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74753136C= , CM000677.2:g.74753136C= GRCh38
NC_000015.9:g.75045477C= , CM000677.1:g.75045477C= GRCh37
NC_000015.8:g.72832530C= NCBI36
NG_008431.1:g.35595C=
NG_008431.2:g.35595C=
NG_061543.1:g.9292C=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1167-48C= MANE Select ENSP00000342007.4:n.1167-48C=
ENST00000343932.4:c.1167-48C= ENSP00000342007.4:n.1167-48C=
NM_000761.4:c.1167-48C= NP_000752.2:n.1167-48C=
NM_000761.5:c.1167-48C= MANE Select NP_000752.2:n.1167-48C=
Search 100 bp 5'
Search 100 bp 3'