Canonical Allele Identifier: CA7660116
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs148212809
ExAC: 15:75047330 G / A
gnomAD v2: 15-75047330-G-A
gnomAD v3: 15-74754989-G-A
gnomAD v4: 15-74754989-G-A
MyVariant Identifiers: chr15:g.75047330G>A (hg19) chr15:g.74754989G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754989G>A , CM000677.2:g.74754989G>A GRCh38
NC_000015.9:g.75047330G>A , CM000677.1:g.75047330G>A GRCh37
NC_000015.8:g.72834383G>A NCBI36
NG_008431.1:g.37448G>A
NG_008431.2:g.37448G>A
NG_061543.1:g.11145G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.1452G>A MANE Select ENSP00000342007.4:p.Pro484=
ENST00000343932.4:c.1452G>A ENSP00000342007.4:p.Pro484=
NM_000761.4:c.1452G>A NP_000752.2:p.Pro484=
NM_000761.5:c.1452G>A MANE Select NP_000752.2:p.Pro484=
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Search 100 bp 3'