Canonical Allele Identifier: CA948672371
Gene: HMGA2 HGNC NCBI

Linked Data

dbSNP Id: rs1876895075
gnomAD v3: 12-65965931-A-C
gnomAD v4: 12-65965931-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65965931A>C , CM000674.2:g.65965931A>C GRCh38
NC_000012.11:g.66359711A>C , CM000674.1:g.66359711A>C GRCh37
NC_000012.10:g.64645978A>C NCBI36
NG_016296.1:g.146472A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.*2639A>C MANE Select ENSP00000384026.2:n.*2639A>C
ENST00000403681.6:c.*2639A>C ENSP00000384026.2:n.*2639A>C
NM_003483.4:c.*2639A>C NP_003474.1:n.*2639A>C
NM_003483.6:c.*2639A>C MANE Select NP_003474.1:n.*2639A>C
Search 100 bp 5'
Search 100 bp 3'