Canonical Allele Identifier: CA2575790280
Gene: CYP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74753147C>T , CM000677.2:g.74753147C>T GRCh38
NC_000015.9:g.75045488C>T , CM000677.1:g.75045488C>T GRCh37
NC_000015.8:g.72832541C>T NCBI36
NG_008431.1:g.35606C>T
NG_008431.2:g.35606C>T
NG_061543.1:g.9303C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1167-37C>T MANE Select ENSP00000342007.4:n.1167-37C>T
ENST00000343932.4:c.1167-37C>T ENSP00000342007.4:n.1167-37C>T
NM_000761.4:c.1167-37C>T NP_000752.2:n.1167-37C>T
NM_000761.5:c.1167-37C>T MANE Select NP_000752.2:n.1167-37C>T
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