Canonical Allele Identifier: CA2187824275
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1862894347
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749078T>A , CM000677.2:g.74749078T>A GRCh38
NC_000015.9:g.75041419T>A , CM000677.1:g.75041419T>A GRCh37
NC_000015.8:g.72828472T>A NCBI36
NG_008431.1:g.31537T>A
NG_008431.2:g.31537T>A
NG_061543.1:g.5234T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.-10+181T>A MANE Select ENSP00000342007.4:n.-10+181T>A
ENST00000343932.4:c.-10+181T>A ENSP00000342007.4:n.-10+181T>A
NM_000761.4:c.-10+181T>A NP_000752.2:n.-10+181T>A
NM_000761.5:c.-10+181T>A MANE Select NP_000752.2:n.-10+181T>A
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