Canonical Allele Identifier: CA691060117

Gene: HMGA2

Linked Data

• dbSNP Id: rs1335222042
• gnomAD v3: 12-65950013-A-G
• gnomAD v4: 12-65950013-A-G
• MyVariant Identifiers: chr12:g.66343793A>G (hg19) ; chr12:g.65950013A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65950013A>G , CM000674.2:g.65950013A>G	GRCh38
NC_000012.11:g.66343793A>G , CM000674.1:g.66343793A>G	GRCh37
NC_000012.10:g.64630060A>G	NCBI36
NG_016296.1:g.130554A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403681.7:c.250-1370A>G MANE Select	ENSP00000384026.2:n.250-1370A>G
ENST00000393577.7:c.250-1370A>G	ENSP00000377205.3:n.250-1370A>G
ENST00000403681.6:c.250-1370A>G	ENSP00000384026.2:n.250-1370A>G
ENST00000539662.1:c.287-1370A>G	ENSP00000440919.1:n.287-1370A>G
ENST00000541363.5:c.250-1370A>G	ENSP00000439317.1:n.250-1370A>G
NM_001300918.1:c.250-1370A>G	NP_001287847.1:n.250-1370A>G
NM_003483.4:c.250-1370A>G	NP_003474.1:n.250-1370A>G
NM_003483.6:c.250-1370A>G MANE Select	NP_003474.1:n.250-1370A>G