Canonical Allele Identifier: CA2187826921
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1596359165
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754544T>G , CM000677.2:g.74754544T>G GRCh38
NC_000015.9:g.75046885T>G , CM000677.1:g.75046885T>G GRCh37
NC_000015.8:g.72833938T>G NCBI36
NG_008431.1:g.37003T>G
NG_008431.2:g.37003T>G
NG_061543.1:g.10700T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1254-247T>G MANE Select ENSP00000342007.4:n.1254-247T>G
ENST00000343932.4:c.1254-247T>G ENSP00000342007.4:n.1254-247T>G
NM_000761.4:c.1254-247T>G NP_000752.2:n.1254-247T>G
NM_000761.5:c.1254-247T>G MANE Select NP_000752.2:n.1254-247T>G
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