Canonical Allele Identifier: CA2187824262
Gene: CYP1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749046G= , CM000677.2:g.74749046G= GRCh38
NC_000015.9:g.75041387G= , CM000677.1:g.75041387G= GRCh37
NC_000015.8:g.72828440G= NCBI36
NG_008431.1:g.31505G=
NG_008431.2:g.31505G=
NG_061543.1:g.5202G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.-10+149G= MANE Select ENSP00000342007.4:n.-10+149G=
ENST00000343932.4:c.-10+149G= ENSP00000342007.4:n.-10+149G=
NM_000761.4:c.-10+149G= NP_000752.2:n.-10+149G=
NM_000761.5:c.-10+149G= MANE Select NP_000752.2:n.-10+149G=
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