Canonical Allele Identifier: CA272820139
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1047230560
gnomAD v2: 15-75041642-C-A
gnomAD v3: 15-74749301-C-A
gnomAD v4: 15-74749301-C-A
MyVariant Identifiers: chr15:g.75041642C>A (hg19) chr15:g.74749301C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74749301C>A , CM000677.2:g.74749301C>A GRCh38
NC_000015.9:g.75041642C>A , CM000677.1:g.75041642C>A GRCh37
NC_000015.8:g.72828695C>A NCBI36
NG_008431.1:g.31760C>A
NG_008431.2:g.31760C>A
NG_061543.1:g.5457C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.-10+404C>A MANE Select ENSP00000342007.4:n.-10+404C>A
ENST00000343932.4:c.-10+404C>A ENSP00000342007.4:n.-10+404C>A
NM_000761.4:c.-10+404C>A NP_000752.2:n.-10+404C>A
NM_000761.5:c.-10+404C>A MANE Select NP_000752.2:n.-10+404C>A
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