Canonical Allele Identifier: CA272816008
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1018366220
MyVariant Identifiers: chr15:g.74754639A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754639A>G , CM000677.2:g.74754639A>G GRCh38
NC_000015.9:g.75046980A>G , CM000677.1:g.75046980A>G GRCh37
NC_000015.8:g.72834033A>G NCBI36
NG_008431.1:g.37098A>G
NG_008431.2:g.37098A>G
NG_061543.1:g.10795A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1254-152A>G MANE Select ENSP00000342007.4:n.1254-152A>G
ENST00000343932.4:c.1254-152A>G ENSP00000342007.4:n.1254-152A>G
NM_000761.4:c.1254-152A>G NP_000752.2:n.1254-152A>G
NM_000761.5:c.1254-152A>G MANE Select NP_000752.2:n.1254-152A>G