Canonical Allele Identifier: CA619412644
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1187887401
gnomAD v2: 15-75047475-C-T
gnomAD v3: 15-74755134-C-T
gnomAD v4: 15-74755134-C-T
MyVariant Identifiers: chr15:g.75047475C>T (hg19) chr15:g.74755134C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755134C>T , CM000677.2:g.74755134C>T GRCh38
NC_000015.9:g.75047475C>T , CM000677.1:g.75047475C>T GRCh37
NC_000015.8:g.72834528C>T NCBI36
NG_008431.1:g.37593C>T
NG_008431.2:g.37593C>T
NG_061543.1:g.11290C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*46C>T MANE Select ENSP00000342007.4:n.*46C>T
ENST00000343932.4:c.*46C>T ENSP00000342007.4:n.*46C>T
NM_000761.4:c.*46C>T NP_000752.2:n.*46C>T
NM_000761.5:c.*46C>T MANE Select NP_000752.2:n.*46C>T
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