Canonical Allele Identifier: CA2189062358

Gene: HMG20A

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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