Canonical Allele Identifier: CA393169506
Gene: CYP1A2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754876A>C , CM000677.2:g.74754876A>C GRCh38
NC_000015.9:g.75047217A>C , CM000677.1:g.75047217A>C GRCh37
NC_000015.8:g.72834270A>C NCBI36
NG_008431.1:g.37335A>C
NG_008431.2:g.37335A>C
NG_061543.1:g.11032A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1339A>C MANE Select ENSP00000342007.4:p.Lys447Gln
ENST00000343932.4:c.1339A>C ENSP00000342007.4:p.Lys447Gln
NM_000761.4:c.1339A>C NP_000752.2:p.Lys447Gln
NM_000761.5:c.1339A>C MANE Select NP_000752.2:p.Lys447Gln