Canonical Allele Identifier: CA2042810736

Gene: HMGA2

Linked Data

• dbSNP Id: rs1876647509

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65957921A>C , CM000674.2:g.65957921A>C	GRCh38
NC_000012.11:g.66351701A>C , CM000674.1:g.66351701A>C	GRCh37
NC_000012.10:g.64637968A>C	NCBI36
NG_016296.1:g.138462A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403681.7:c.283-5324A>C MANE Select	ENSP00000384026.2:n.283-5324A>C
ENST00000403681.6:c.283-5324A>C	ENSP00000384026.2:n.283-5324A>C
ENST00000539662.1:c.320-5324A>C	ENSP00000440919.1:n.320-5324A>C
ENST00000541363.5:c.*6488A>C	ENSP00000439317.1:n.*6488A>C
NM_003483.4:c.283-5324A>C	NP_003474.1:n.283-5324A>C
NM_003483.6:c.283-5324A>C MANE Select	NP_003474.1:n.283-5324A>C