Canonical Allele Identifier: CA2042783149

Gene: HMGA2

Linked Data

• dbSNP Id: rs1876404869

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65950069A>G , CM000674.2:g.65950069A>G	GRCh38
NC_000012.11:g.66343849A>G , CM000674.1:g.66343849A>G	GRCh37
NC_000012.10:g.64630116A>G	NCBI36
NG_016296.1:g.130610A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000403681.7:c.250-1314A>G MANE Select	ENSP00000384026.2:n.250-1314A>G
ENST00000393577.7:c.250-1314A>G	ENSP00000377205.3:n.250-1314A>G
ENST00000403681.6:c.250-1314A>G	ENSP00000384026.2:n.250-1314A>G
ENST00000539662.1:c.287-1314A>G	ENSP00000440919.1:n.287-1314A>G
ENST00000541363.5:c.250-1314A>G	ENSP00000439317.1:n.250-1314A>G
NM_001300918.1:c.250-1314A>G	NP_001287847.1:n.250-1314A>G
NM_003483.4:c.250-1314A>G	NP_003474.1:n.250-1314A>G
NM_003483.6:c.250-1314A>G MANE Select	NP_003474.1:n.250-1314A>G