Canonical Allele Identifier: CA2187825587
Gene: CYP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74751861G= , CM000677.2:g.74751861G= GRCh38
NC_000015.9:g.75044202G= , CM000677.1:g.75044202G= GRCh37
NC_000015.8:g.72831255G= NCBI36
NG_008431.1:g.34320G=
NG_008431.2:g.34320G=
NG_061543.1:g.8017G=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1042+7G= MANE Select ENSP00000342007.4:n.1042+7G=
ENST00000343932.4:c.1042+7G= ENSP00000342007.4:n.1042+7G=
NM_000761.4:c.1042+7G= NP_000752.2:n.1042+7G=
NM_000761.5:c.1042+7G= MANE Select NP_000752.2:n.1042+7G=
Search 100 bp 5'
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