Canonical Allele Identifier: CA605678791

Gene: HMGA2

Linked Data

• dbSNP Id: rs181717035
• gnomAD v2: 12-66343922-G-A
• MyVariant Identifiers: chr12:g.66343922G>A (hg19) ; chr12:g.65950142G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.65950142G>A , CM000674.2:g.65950142G>A	GRCh38
NC_000012.11:g.66343922G>A , CM000674.1:g.66343922G>A	GRCh37
NC_000012.10:g.64630189G>A	NCBI36
NG_016296.1:g.130683G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000403681.7:c.250-1241G>A MANE Select	ENSP00000384026.2:n.250-1241G>A
ENST00000393577.7:c.250-1241G>A	ENSP00000377205.3:n.250-1241G>A
ENST00000403681.6:c.250-1241G>A	ENSP00000384026.2:n.250-1241G>A
ENST00000539662.1:c.287-1241G>A	ENSP00000440919.1:n.287-1241G>A
ENST00000541363.5:c.250-1241G>A	ENSP00000439317.1:n.250-1241G>A
NM_001300918.1:c.250-1241G>A	NP_001287847.1:n.250-1241G>A
NM_003483.4:c.250-1241G>A	NP_003474.1:n.250-1241G>A
NM_003483.6:c.250-1241G>A MANE Select	NP_003474.1:n.250-1241G>A