Canonical Allele Identifier: CA2804766362
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754709C>T , CM000677.2:g.74754709C>T GRCh38
NC_000015.9:g.75047050C>T , CM000677.1:g.75047050C>T GRCh37
NC_000015.8:g.72834103C>T NCBI36
NG_008431.1:g.37168C>T
NG_008431.2:g.37168C>T
NG_061543.1:g.10865C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1254-82C>T MANE Select ENSP00000342007.4:n.1254-82C>T
ENST00000343932.4:c.1254-82C>T ENSP00000342007.4:n.1254-82C>T
NM_000761.4:c.1254-82C>T NP_000752.2:n.1254-82C>T
NM_000761.5:c.1254-82C>T MANE Select NP_000752.2:n.1254-82C>T