Canonical Allele Identifier: CA2619689507
Gene: HMGA2 HGNC NCBI

Linked Data

gnomAD v4: 12-65957992-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65957992G>T , CM000674.2:g.65957992G>T GRCh38
NC_000012.11:g.66351772G>T , CM000674.1:g.66351772G>T GRCh37
NC_000012.10:g.64638039G>T NCBI36
NG_016296.1:g.138533G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.283-5253G>T MANE Select ENSP00000384026.2:n.283-5253G>T
ENST00000403681.6:c.283-5253G>T ENSP00000384026.2:n.283-5253G>T
ENST00000539662.1:c.320-5253G>T ENSP00000440919.1:n.320-5253G>T
ENST00000541363.5:c.*6559G>T ENSP00000439317.1:n.*6559G>T
NM_003483.4:c.283-5253G>T NP_003474.1:n.283-5253G>T
NM_003483.6:c.283-5253G>T MANE Select NP_003474.1:n.283-5253G>T
Search 100 bp 5'
Search 100 bp 3'