Canonical Allele Identifier: CA2187826231
Gene: CYP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74753153T= , CM000677.2:g.74753153T= GRCh38
NC_000015.9:g.75045494T= , CM000677.1:g.75045494T= GRCh37
NC_000015.8:g.72832547T= NCBI36
NG_008431.1:g.35612T=
NG_008431.2:g.35612T=
NG_061543.1:g.9309T=

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1167-31T= MANE Select ENSP00000342007.4:n.1167-31T=
ENST00000343932.4:c.1167-31T= ENSP00000342007.4:n.1167-31T=
NM_000761.4:c.1167-31T= NP_000752.2:n.1167-31T=
NM_000761.5:c.1167-31T= MANE Select NP_000752.2:n.1167-31T=
Search 100 bp 5'
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