Canonical Allele Identifier: CA619123148
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1248862345
gnomAD v2: 15-75047703-C-CA
gnomAD v3: 15-74755362-C-CA
gnomAD v4: 15-74755362-C-CA
MyVariant Identifiers: chr15:g.75047704_75047705insA (hg19) chr15:g.75047703_75047704insA (hg19) chr15:g.74755363_74755364insA (hg38) chr15:g.74755362_74755363insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755365dup , CM000677.2:g.74755365dup GRCh38
NC_000015.9:g.75047706dup , CM000677.1:g.75047706dup GRCh37
NC_000015.8:g.72834759dup NCBI36
NG_008431.1:g.37824dup
NG_008431.2:g.37824dup
NG_061543.1:g.11521dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*277dup MANE Select ENSP00000342007.4:n.*277dup
ENST00000343932.4:c.*277dup ENSP00000342007.4:n.*277dup
NM_000761.4:c.*277dup NP_000752.2:n.*277dup
NM_000761.5:c.*277dup MANE Select NP_000752.2:n.*277dup
Search 100 bp 5'
Search 100 bp 3'