Canonical Allele Identifier: CA2547079184
Gene: HMGA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65950111C>A , CM000674.2:g.65950111C>A GRCh38
NC_000012.11:g.66343891C>A , CM000674.1:g.66343891C>A GRCh37
NC_000012.10:g.64630158C>A NCBI36
NG_016296.1:g.130652C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.250-1272C>A MANE Select ENSP00000384026.2:n.250-1272C>A
ENST00000393577.7:c.250-1272C>A ENSP00000377205.3:n.250-1272C>A
ENST00000403681.6:c.250-1272C>A ENSP00000384026.2:n.250-1272C>A
ENST00000539662.1:c.287-1272C>A ENSP00000440919.1:n.287-1272C>A
ENST00000541363.5:c.250-1272C>A ENSP00000439317.1:n.250-1272C>A
NM_001300918.1:c.250-1272C>A NP_001287847.1:n.250-1272C>A
NM_003483.4:c.250-1272C>A NP_003474.1:n.250-1272C>A
NM_003483.6:c.250-1272C>A MANE Select NP_003474.1:n.250-1272C>A
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