Canonical Allele Identifier: CA2042809302
Gene: HMGA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65955977A= , CM000674.2:g.65955977A= GRCh38
NC_000012.11:g.66349757A= , CM000674.1:g.66349757A= GRCh37
NC_000012.10:g.64636024A= NCBI36
NG_016296.1:g.136518A=

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.282+4562A= MANE Select ENSP00000384026.2:n.282+4562A=
ENST00000403681.6:c.282+4562A= ENSP00000384026.2:n.282+4562A=
ENST00000539662.1:c.319+4562A= ENSP00000440919.1:n.319+4562A=
ENST00000541363.5:c.*4544A= ENSP00000439317.1:n.*4544A=
NM_003483.4:c.282+4562A= NP_003474.1:n.282+4562A=
NM_003483.6:c.282+4562A= MANE Select NP_003474.1:n.282+4562A=
Search 100 bp 5'
Search 100 bp 3'