Canonical Allele Identifier: CA2042783200
Gene: HMGA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65950094A= , CM000674.2:g.65950094A= GRCh38
NC_000012.11:g.66343874A= , CM000674.1:g.66343874A= GRCh37
NC_000012.10:g.64630141A= NCBI36
NG_016296.1:g.130635A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403681.7:c.250-1289A= MANE Select ENSP00000384026.2:n.250-1289A=
ENST00000393577.7:c.250-1289A= ENSP00000377205.3:n.250-1289A=
ENST00000403681.6:c.250-1289A= ENSP00000384026.2:n.250-1289A=
ENST00000539662.1:c.287-1289A= ENSP00000440919.1:n.287-1289A=
ENST00000541363.5:c.250-1289A= ENSP00000439317.1:n.250-1289A=
NM_001300918.1:c.250-1289A= NP_001287847.1:n.250-1289A=
NM_003483.4:c.250-1289A= NP_003474.1:n.250-1289A=
NM_003483.6:c.250-1289A= MANE Select NP_003474.1:n.250-1289A=
Search 100 bp 5'
Search 100 bp 3'