Canonical Allele Identifier: CA2042817520
Gene: HMGA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65965912T= , CM000674.2:g.65965912T= GRCh38
NC_000012.11:g.66359692T= , CM000674.1:g.66359692T= GRCh37
NC_000012.10:g.64645959T= NCBI36
NG_016296.1:g.146453T=

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.*2620T= MANE Select ENSP00000384026.2:n.*2620T=
ENST00000403681.6:c.*2620T= ENSP00000384026.2:n.*2620T=
NM_003483.4:c.*2620T= NP_003474.1:n.*2620T=
NM_003483.6:c.*2620T= MANE Select NP_003474.1:n.*2620T=