Canonical Allele Identifier: CA2042817491
Gene: HMGA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65965872A= , CM000674.2:g.65965872A= GRCh38
NC_000012.11:g.66359652A= , CM000674.1:g.66359652A= GRCh37
NC_000012.10:g.64645919A= NCBI36
NG_016296.1:g.146413A=

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.*2580A= MANE Select ENSP00000384026.2:n.*2580A=
ENST00000403681.6:c.*2580A= ENSP00000384026.2:n.*2580A=
NM_003483.4:c.*2580A= NP_003474.1:n.*2580A=
NM_003483.6:c.*2580A= MANE Select NP_003474.1:n.*2580A=
Search 100 bp 5'
Search 100 bp 3'