Canonical Allele Identifier: CA2042816367
Gene: HMGA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964396A= , CM000674.2:g.65964396A= GRCh38
NC_000012.11:g.66358176A= , CM000674.1:g.66358176A= GRCh37
NC_000012.10:g.64644443A= NCBI36
NG_016296.1:g.144937A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403681.7:c.*1104A= MANE Select ENSP00000384026.2:n.*1104A=
ENST00000403681.6:c.*1104A= ENSP00000384026.2:n.*1104A=
NM_003483.4:c.*1104A= NP_003474.1:n.*1104A=
NM_003483.6:c.*1104A= MANE Select NP_003474.1:n.*1104A=
Search 100 bp 5'
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