Canonical Allele Identifier: CA7660101
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs535377637
ExAC: 15:75047264 C / A
gnomAD v2: 15-75047264-C-A
gnomAD v3: 15-74754923-C-A
gnomAD v4: 15-74754923-C-A
MyVariant Identifiers: chr15:g.75047264C>A (hg19) chr15:g.74754923C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754923C>A , CM000677.2:g.74754923C>A GRCh38
NC_000015.9:g.75047264C>A , CM000677.1:g.75047264C>A GRCh37
NC_000015.8:g.72834317C>A NCBI36
NG_008431.1:g.37382C>A
NG_008431.2:g.37382C>A
NG_061543.1:g.11079C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1386C>A MANE Select ENSP00000342007.4:p.Val462=
ENST00000343932.4:c.1386C>A ENSP00000342007.4:p.Val462=
NM_000761.4:c.1386C>A NP_000752.2:p.Val462=
NM_000761.5:c.1386C>A MANE Select NP_000752.2:p.Val462=
Search 100 bp 5'
Search 100 bp 3'