Canonical Allele Identifier: CA619123191
Gene: CYP1A2 HGNC NCBI

Linked Data

dbSNP Id: rs150722579
gnomAD v2: 15-75047721-A-ACC
gnomAD v3: 15-74755380-A-ACC
gnomAD v4: 15-74755380-A-ACC
MyVariant Identifiers: chr15:g.75047721_75047722insCC (hg19) chr15:g.74755380_74755381insCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74755381_74755382dup , CM000677.2:g.74755381_74755382dup GRCh38
NC_000015.9:g.75047722_75047723dup , CM000677.1:g.75047722_75047723dup GRCh37
NC_000015.8:g.72834775_72834776dup NCBI36
NG_008431.1:g.37840_37841dup
NG_008431.2:g.37840_37841dup
NG_061543.1:g.11537_11538dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000343932.5:c.*293_*294dup MANE Select ENSP00000342007.4:n.*293_*294dup
ENST00000343932.4:c.*293_*294dup ENSP00000342007.4:n.*293_*294dup
NM_000761.4:c.*293_*294dup NP_000752.2:n.*293_*294dup
NM_000761.5:c.*293_*294dup MANE Select NP_000752.2:n.*293_*294dup
Search 100 bp 5'
Search 100 bp 3'