Canonical Allele Identifier: CA2042810760
Gene: HMGA2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.65957980A= , CM000674.2:g.65957980A= GRCh38
NC_000012.11:g.66351760A= , CM000674.1:g.66351760A= GRCh37
NC_000012.10:g.64638027A= NCBI36
NG_016296.1:g.138521A=

Transcript Alleles

HGVS Amino-acid change
ENST00000403681.7:c.283-5265A= MANE Select ENSP00000384026.2:n.283-5265A=
ENST00000403681.6:c.283-5265A= ENSP00000384026.2:n.283-5265A=
ENST00000539662.1:c.320-5265A= ENSP00000440919.1:n.320-5265A=
ENST00000541363.5:c.*6547A= ENSP00000439317.1:n.*6547A=
NM_003483.4:c.283-5265A= NP_003474.1:n.283-5265A=
NM_003483.6:c.283-5265A= MANE Select NP_003474.1:n.283-5265A=
Search 100 bp 5'
Search 100 bp 3'