Canonical Allele Identifier: CA2042817513
Gene: HMGA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65965905T= , CM000674.2:g.65965905T= GRCh38
NC_000012.11:g.66359685T= , CM000674.1:g.66359685T= GRCh37
NC_000012.10:g.64645952T= NCBI36
NG_016296.1:g.146446T=

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.*2613T= MANE Select ENSP00000384026.2:n.*2613T=
ENST00000403681.6:c.*2613T= ENSP00000384026.2:n.*2613T=
NM_003483.4:c.*2613T= NP_003474.1:n.*2613T=
NM_003483.6:c.*2613T= MANE Select NP_003474.1:n.*2613T=
Search 100 bp 5'
Search 100 bp 3'