Canonical Allele Identifier: CA13623913
Gene: HMGA2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10784502

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65950030C>T , CM000674.2:g.65950030C>T GRCh38
NC_000012.10:g.64630077C>T NCBI36
NC_000012.11:g.66343810C>T , CM000674.1:g.66343810C>T GRCh37
NG_016296.1:g.130571C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000393577.7:c.250-1353C>T ENSP00000377205.3:p.=
ENST00000403681.6:c.250-1353C>T ENSP00000384026.2:p.=
ENST00000539662.1:n.287-1353C>T ENSP00000440919.1:p.=
ENST00000541363.5:c.250-1353C>T ENSP00000439317.1:p.=
NM_001300918.1:c.250-1353C>T VV NP_001287847.1:p.=
NM_003483.4:c.250-1353C>T VV NP_003474.1:p.=