Canonical Allele Identifier: CA15836869

Gene: HMG20A

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.77454848A>G , CM000677.2:g.77454848A>G	GRCh38
NC_000015.9:g.77747190A>G , CM000677.1:g.77747190A>G	GRCh37
NC_000015.8:g.75534245A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336216.9:c.-4-3556A>G MANE Select	ENSP00000336856.4:n.-4-3556A>G
ENST00000336216.8:c.-4-3556A>G	ENSP00000336856.4:n.-4-3556A>G
ENST00000381714.7:c.-4-3556A>G	ENSP00000371133.3:n.-4-3556A>G
ENST00000558176.1:c.-317-3556A>G	ENSP00000452665.1:n.-317-3556A>G
ENST00000558651.5:c.-293-3606A>G	ENSP00000453727.1:n.-293-3606A>G
ENST00000559035.5:c.-4-3556A>G	ENSP00000453592.1:n.-4-3556A>G
ENST00000559099.5:c.-4-3556A>G	ENSP00000454136.1:n.-4-3556A>G
ENST00000560498.5:c.-4-3556A>G	ENSP00000453498.1:n.-4-3556A>G
ENST00000560986.1:n.71-3556A>G
NM_001304504.1:c.-4-3556A>G	NP_001291433.1:n.-4-3556A>G
NM_001304505.1:c.-255-3556A>G	NP_001291434.1:n.-255-3556A>G
NM_018200.3:c.-4-3556A>G	NP_060670.1:n.-4-3556A>G
XM_011521158.1:c.-4-3556A>G	XP_011519460.1:n.-4-3556A>G
XM_011521158.3:c.-4-3556A>G	XP_011519460.1:n.-4-3556A>G
XR_001751049.2:n.301-3556A>G
NM_001304504.2:c.-4-3556A>G MANE Select	NP_001291433.1:n.-4-3556A>G
NM_001304505.2:c.-255-3556A>G	NP_001291434.1:n.-255-3556A>G
NM_018200.4:c.-4-3556A>G	NP_060670.1:n.-4-3556A>G