Canonical Allele Identifier: CA7659716
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs779919195
ExAC: 15:75042304 C / G
gnomAD v2: 15-75042304-C-G
gnomAD v4: 15-74749963-C-G
MyVariant Identifiers: chr15:g.75042304C>G (hg19) chr15:g.74749963C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749963C>G , CM000677.2:g.74749963C>G GRCh38
NC_000015.9:g.75042304C>G , CM000677.1:g.75042304C>G GRCh37
NC_000015.8:g.72829357C>G NCBI36
NG_008431.1:g.32422C>G
NG_008431.2:g.32422C>G
NG_061543.1:g.6119C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.225C>G MANE Select ENSP00000342007.4:p.Val75=
ENST00000343932.4:c.225C>G ENSP00000342007.4:p.Val75=
NM_000761.4:c.225C>G NP_000752.2:p.Val75=
NM_000761.5:c.225C>G MANE Select NP_000752.2:p.Val75=
Search 100 bp 5'
Search 100 bp 3'