Canonical Allele Identifier: CA2042782885
Gene: HMGA2 HGNC NCBI

Linked Data

dbSNP Id: rs1417781911
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65949879A>T , CM000674.2:g.65949879A>T GRCh38
NC_000012.11:g.66343659A>T , CM000674.1:g.66343659A>T GRCh37
NC_000012.10:g.64629926A>T NCBI36
NG_016296.1:g.130420A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.250-1504A>T MANE Select ENSP00000384026.2:n.250-1504A>T
ENST00000393577.7:c.250-1504A>T ENSP00000377205.3:n.250-1504A>T
ENST00000403681.6:c.250-1504A>T ENSP00000384026.2:n.250-1504A>T
ENST00000539662.1:c.287-1504A>T ENSP00000440919.1:n.287-1504A>T
ENST00000541363.5:c.250-1504A>T ENSP00000439317.1:n.250-1504A>T
NM_001300918.1:c.250-1504A>T NP_001287847.1:n.250-1504A>T
NM_003483.4:c.250-1504A>T NP_003474.1:n.250-1504A>T
NM_003483.6:c.250-1504A>T MANE Select NP_003474.1:n.250-1504A>T
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