Canonical Allele Identifier: CA238996363
Gene: HMGA2 HGNC NCBI

Linked Data

dbSNP Id: rs774399701
gnomAD v2: 12-66358397-A-AG
gnomAD v3: 12-65964617-A-AG
gnomAD v4: 12-65964617-A-AG
MyVariant Identifiers: chr12:g.66358397_66358398insG (hg19) chr12:g.65964617_65964618insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964618dup , CM000674.2:g.65964618dup GRCh38
NC_000012.11:g.66358398dup , CM000674.1:g.66358398dup GRCh37
NC_000012.10:g.64644665dup NCBI36
NG_016296.1:g.145159dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000403681.7:c.*1326dup MANE Select ENSP00000384026.2:n.*1326dup
ENST00000403681.6:c.*1326dup ENSP00000384026.2:n.*1326dup
NM_003483.4:c.*1326dup NP_003474.1:n.*1326dup
NM_003483.6:c.*1326dup MANE Select NP_003474.1:n.*1326dup
Search 100 bp 5'
Search 100 bp 3'