Canonical Allele Identifier: CA2042776051
Gene: HMGA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65944422G>A , CM000674.2:g.65944422G>A GRCh38
NC_000012.11:g.66338202G>A , CM000674.1:g.66338202G>A GRCh37
NC_000012.10:g.64624469G>A NCBI36
NG_016296.1:g.124963G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000403681.7:c.250-6961G>A MANE Select ENSP00000384026.2:n.250-6961G>A
ENST00000393577.7:c.250-6961G>A ENSP00000377205.3:n.250-6961G>A
ENST00000403681.6:c.250-6961G>A ENSP00000384026.2:n.250-6961G>A
ENST00000539662.1:c.287-6961G>A ENSP00000440919.1:n.287-6961G>A
ENST00000541363.5:c.250-6961G>A ENSP00000439317.1:n.250-6961G>A
NM_001300918.1:c.250-6961G>A NP_001287847.1:n.250-6961G>A
NM_003483.4:c.250-6961G>A NP_003474.1:n.250-6961G>A
NM_003483.6:c.250-6961G>A MANE Select NP_003474.1:n.250-6961G>A
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