Canonical Allele Identifier: CA691066213
Gene: HMGA2 HGNC NCBI

Linked Data

dbSNP Id: rs1437316106
MyVariant Identifiers: chr12:g.66358405A>T (hg19) chr12:g.65964625A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964625A>T , CM000674.2:g.65964625A>T GRCh38
NC_000012.11:g.66358405A>T , CM000674.1:g.66358405A>T GRCh37
NC_000012.10:g.64644672A>T NCBI36
NG_016296.1:g.145166A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.*1333A>T MANE Select ENSP00000384026.2:n.*1333A>T
ENST00000403681.6:c.*1333A>T ENSP00000384026.2:n.*1333A>T
NM_003483.4:c.*1333A>T NP_003474.1:n.*1333A>T
NM_003483.6:c.*1333A>T MANE Select NP_003474.1:n.*1333A>T
Search 100 bp 5'
Search 100 bp 3'