Canonical Allele Identifier: CA2042809283
Gene: HMGA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65955945T= , CM000674.2:g.65955945T= GRCh38
NC_000012.11:g.66349725T= , CM000674.1:g.66349725T= GRCh37
NC_000012.10:g.64635992T= NCBI36
NG_016296.1:g.136486T=

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.282+4530T= MANE Select ENSP00000384026.2:n.282+4530T=
ENST00000403681.6:c.282+4530T= ENSP00000384026.2:n.282+4530T=
ENST00000539662.1:c.319+4530T= ENSP00000440919.1:n.319+4530T=
ENST00000541363.5:c.*4512T= ENSP00000439317.1:n.*4512T=
NM_003483.4:c.282+4530T= NP_003474.1:n.282+4530T=
NM_003483.6:c.282+4530T= MANE Select NP_003474.1:n.282+4530T=
Search 100 bp 5'
Search 100 bp 3'