Canonical Allele Identifier: CA2042809300

Gene: HMGA2

Linked Data

• dbSNP Id: rs1555189209

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65955970T>G , CM000674.2:g.65955970T>G	GRCh38
NC_000012.11:g.66349750T>G , CM000674.1:g.66349750T>G	GRCh37
NC_000012.10:g.64636017T>G	NCBI36
NG_016296.1:g.136511T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403681.7:c.282+4555T>G MANE Select	ENSP00000384026.2:n.282+4555T>G
ENST00000403681.6:c.282+4555T>G	ENSP00000384026.2:n.282+4555T>G
ENST00000539662.1:c.319+4555T>G	ENSP00000440919.1:n.319+4555T>G
ENST00000541363.5:c.*4537T>G	ENSP00000439317.1:n.*4537T>G
NM_003483.4:c.282+4555T>G	NP_003474.1:n.282+4555T>G
NM_003483.6:c.282+4555T>G MANE Select	NP_003474.1:n.282+4555T>G