Canonical Allele Identifier: CA2187826995
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs2063330062
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754712C>G , CM000677.2:g.74754712C>G GRCh38
NC_000015.9:g.75047053C>G , CM000677.1:g.75047053C>G GRCh37
NC_000015.8:g.72834106C>G NCBI36
NG_008431.1:g.37171C>G
NG_008431.2:g.37171C>G
NG_061543.1:g.10868C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1254-79C>G MANE Select ENSP00000342007.4:n.1254-79C>G
ENST00000343932.4:c.1254-79C>G ENSP00000342007.4:n.1254-79C>G
NM_000761.4:c.1254-79C>G NP_000752.2:n.1254-79C>G
NM_000761.5:c.1254-79C>G MANE Select NP_000752.2:n.1254-79C>G
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