Canonical Allele Identifier: CA691066216
Gene: HMGA2 HGNC NCBI

Linked Data

dbSNP Id: rs1183838139
gnomAD v3: 12-65964634-G-T
gnomAD v4: 12-65964634-G-T
MyVariant Identifiers: chr12:g.66358414G>T (hg19) chr12:g.65964634G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964634G>T , CM000674.2:g.65964634G>T GRCh38
NC_000012.11:g.66358414G>T , CM000674.1:g.66358414G>T GRCh37
NC_000012.10:g.64644681G>T NCBI36
NG_016296.1:g.145175G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.*1342G>T MANE Select ENSP00000384026.2:n.*1342G>T
ENST00000403681.6:c.*1342G>T ENSP00000384026.2:n.*1342G>T
NM_003483.4:c.*1342G>T NP_003474.1:n.*1342G>T
NM_003483.6:c.*1342G>T MANE Select NP_003474.1:n.*1342G>T
Search 100 bp 5'
Search 100 bp 3'