Canonical Allele Identifier: CA2619689086
Gene: HMGA2 HGNC NCBI

Linked Data

gnomAD v4: 12-65955936-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65955936G>T , CM000674.2:g.65955936G>T GRCh38
NC_000012.11:g.66349716G>T , CM000674.1:g.66349716G>T GRCh37
NC_000012.10:g.64635983G>T NCBI36
NG_016296.1:g.136477G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.282+4521G>T MANE Select ENSP00000384026.2:n.282+4521G>T
ENST00000403681.6:c.282+4521G>T ENSP00000384026.2:n.282+4521G>T
ENST00000539662.1:c.319+4521G>T ENSP00000440919.1:n.319+4521G>T
ENST00000541363.5:c.*4503G>T ENSP00000439317.1:n.*4503G>T
NM_003483.4:c.282+4521G>T NP_003474.1:n.282+4521G>T
NM_003483.6:c.282+4521G>T MANE Select NP_003474.1:n.282+4521G>T
Search 100 bp 5'
Search 100 bp 3'