Canonical Allele Identifier: CA619121379
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1450656899

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749612T>C , CM000677.2:g.74749612T>C GRCh38
NC_000015.9:g.75041953T>C , CM000677.1:g.75041953T>C GRCh37
NC_000015.8:g.72829006T>C NCBI36
NG_008431.1:g.32071T>C
NG_008431.2:g.32071T>C
NG_061543.1:g.5768T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-9-118T>C MANE Select ENSP00000342007.4:n.-9-118T>C
ENST00000343932.4:c.-9-118T>C ENSP00000342007.4:n.-9-118T>C
NM_000761.4:c.-9-118T>C NP_000752.2:n.-9-118T>C
NM_000761.5:c.-9-118T>C MANE Select NP_000752.2:n.-9-118T>C