Canonical Allele Identifier: CA2042782613
Gene: HMGA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65949706T= , CM000674.2:g.65949706T= GRCh38
NC_000012.11:g.66343486T= , CM000674.1:g.66343486T= GRCh37
NC_000012.10:g.64629753T= NCBI36
NG_016296.1:g.130247T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000403681.7:c.250-1677T= MANE Select ENSP00000384026.2:n.250-1677T=
ENST00000393577.7:c.250-1677T= ENSP00000377205.3:n.250-1677T=
ENST00000403681.6:c.250-1677T= ENSP00000384026.2:n.250-1677T=
ENST00000539662.1:c.287-1677T= ENSP00000440919.1:n.287-1677T=
ENST00000541363.5:c.250-1677T= ENSP00000439317.1:n.250-1677T=
NM_001300918.1:c.250-1677T= NP_001287847.1:n.250-1677T=
NM_003483.4:c.250-1677T= NP_003474.1:n.250-1677T=
NM_003483.6:c.250-1677T= MANE Select NP_003474.1:n.250-1677T=
Search 100 bp 5'
Search 100 bp 3'