Canonical Allele Identifier: CA2619690364
Gene: HMGA2 HGNC NCBI

Linked Data

gnomAD v4: 12-65964388-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964388T>A , CM000674.2:g.65964388T>A GRCh38
NC_000012.11:g.66358168T>A , CM000674.1:g.66358168T>A GRCh37
NC_000012.10:g.64644435T>A NCBI36
NG_016296.1:g.144929T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000403681.7:c.*1096T>A MANE Select ENSP00000384026.2:n.*1096T>A
ENST00000403681.6:c.*1096T>A ENSP00000384026.2:n.*1096T>A
NM_003483.4:c.*1096T>A NP_003474.1:n.*1096T>A
NM_003483.6:c.*1096T>A MANE Select NP_003474.1:n.*1096T>A
Search 100 bp 5'
Search 100 bp 3'