Canonical Allele Identifier: CA7660163
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs765991934
ExAC: 15:75047477 C / A
gnomAD v2: 15-75047477-C-A
gnomAD v3: 15-74755136-C-A
gnomAD v4: 15-74755136-C-A
MyVariant Identifiers: chr15:g.75047477C>A (hg19) chr15:g.74755136C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755136C>A , CM000677.2:g.74755136C>A GRCh38
NC_000015.9:g.75047477C>A , CM000677.1:g.75047477C>A GRCh37
NC_000015.8:g.72834530C>A NCBI36
NG_008431.1:g.37595C>A
NG_008431.2:g.37595C>A
NG_061543.1:g.11292C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*48C>A MANE Select ENSP00000342007.4:n.*48C>A
ENST00000343932.4:c.*48C>A ENSP00000342007.4:n.*48C>A
NM_000761.4:c.*48C>A NP_000752.2:n.*48C>A
NM_000761.5:c.*48C>A MANE Select NP_000752.2:n.*48C>A
Search 100 bp 5'
Search 100 bp 3'