Canonical Allele Identifier: CA691063356
Gene: HMGA2 HGNC NCBI

Linked Data

dbSNP Id: rs1379841078
gnomAD v4: 12-65957961-A-G
MyVariant Identifiers: chr12:g.66351741A>G (hg19) chr12:g.65957961A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65957961A>G , CM000674.2:g.65957961A>G GRCh38
NC_000012.11:g.66351741A>G , CM000674.1:g.66351741A>G GRCh37
NC_000012.10:g.64638008A>G NCBI36
NG_016296.1:g.138502A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.283-5284A>G MANE Select ENSP00000384026.2:n.283-5284A>G
ENST00000403681.6:c.283-5284A>G ENSP00000384026.2:n.283-5284A>G
ENST00000539662.1:c.320-5284A>G ENSP00000440919.1:n.320-5284A>G
ENST00000541363.5:c.*6528A>G ENSP00000439317.1:n.*6528A>G
NM_003483.4:c.283-5284A>G NP_003474.1:n.283-5284A>G
NM_003483.6:c.283-5284A>G MANE Select NP_003474.1:n.283-5284A>G
Search 100 bp 5'
Search 100 bp 3'