Canonical Allele Identifier: CA2551760238
Gene: HMGA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65965927G>A , CM000674.2:g.65965927G>A GRCh38
NC_000012.11:g.66359707G>A , CM000674.1:g.66359707G>A GRCh37
NC_000012.10:g.64645974G>A NCBI36
NG_016296.1:g.146468G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.*2635G>A MANE Select ENSP00000384026.2:n.*2635G>A
ENST00000403681.6:c.*2635G>A ENSP00000384026.2:n.*2635G>A
NM_003483.4:c.*2635G>A NP_003474.1:n.*2635G>A
NM_003483.6:c.*2635G>A MANE Select NP_003474.1:n.*2635G>A
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