Canonical Allele Identifier: CA7659971
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs758282308

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74752128T>C , CM000677.2:g.74752128T>C GRCh38
NC_000015.9:g.75044469T>C , CM000677.1:g.75044469T>C GRCh37
NC_000015.8:g.72831522T>C NCBI36
NG_008431.1:g.34587T>C
NG_008431.2:g.34587T>C
NG_061543.1:g.8284T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1047T>C MANE Select ENSP00000342007.4:p.Thr349=
ENST00000343932.4:c.1047T>C ENSP00000342007.4:p.Thr349=
NM_000761.4:c.1047T>C NP_000752.2:p.Thr349=
NM_000761.5:c.1047T>C MANE Select NP_000752.2:p.Thr349=