Canonical Allele Identifier: CA2619690401
Gene: HMGA2 HGNC NCBI

Linked Data

gnomAD v4: 12-65964544-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65964544A>G , CM000674.2:g.65964544A>G GRCh38
NC_000012.11:g.66358324A>G , CM000674.1:g.66358324A>G GRCh37
NC_000012.10:g.64644591A>G NCBI36
NG_016296.1:g.145085A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000403681.7:c.*1252A>G MANE Select ENSP00000384026.2:n.*1252A>G
ENST00000403681.6:c.*1252A>G ENSP00000384026.2:n.*1252A>G
NM_003483.4:c.*1252A>G NP_003474.1:n.*1252A>G
NM_003483.6:c.*1252A>G MANE Select NP_003474.1:n.*1252A>G
Search 100 bp 5'
Search 100 bp 3'