Canonical Allele Identifier: CA2042810758
Gene: HMGA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65957979T= , CM000674.2:g.65957979T= GRCh38
NC_000012.11:g.66351759T= , CM000674.1:g.66351759T= GRCh37
NC_000012.10:g.64638026T= NCBI36
NG_016296.1:g.138520T=

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.283-5266T= MANE Select ENSP00000384026.2:n.283-5266T=
ENST00000403681.6:c.283-5266T= ENSP00000384026.2:n.283-5266T=
ENST00000539662.1:c.320-5266T= ENSP00000440919.1:n.320-5266T=
ENST00000541363.5:c.*6546T= ENSP00000439317.1:n.*6546T=
NM_003483.4:c.283-5266T= NP_003474.1:n.283-5266T=
NM_003483.6:c.283-5266T= MANE Select NP_003474.1:n.283-5266T=
Search 100 bp 5'
Search 100 bp 3'