Canonical Allele Identifier: CA2545989364

Gene: HMGA2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65955959A>G , CM000674.2:g.65955959A>G	GRCh38
NC_000012.11:g.66349739A>G , CM000674.1:g.66349739A>G	GRCh37
NC_000012.10:g.64636006A>G	NCBI36
NG_016296.1:g.136500A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403681.7:c.282+4544A>G MANE Select	ENSP00000384026.2:n.282+4544A>G
ENST00000403681.6:c.282+4544A>G	ENSP00000384026.2:n.282+4544A>G
ENST00000539662.1:c.319+4544A>G	ENSP00000440919.1:n.319+4544A>G
ENST00000541363.5:c.*4526A>G	ENSP00000439317.1:n.*4526A>G
NM_003483.4:c.282+4544A>G	NP_003474.1:n.282+4544A>G
NM_003483.6:c.282+4544A>G MANE Select	NP_003474.1:n.282+4544A>G