Canonical Allele Identifier: CA10604901

Gene: COL6A2

Linked Data

• ClinVar Variation Id: 284768
• ClinVar RCV Id: RCV000384759 ; RCV001216066
• dbSNP Id: rs886042943
• MyVariant Identifiers: chr21:g.47533971G>A (hg19) ; chr21:g.46114057G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46114057G>A , CM000683.2:g.46114057G>A	GRCh38
NC_000021.8:g.47533971G>A , CM000683.1:g.47533971G>A	GRCh37
NC_000021.7:g.46358399G>A	NCBI36
NG_008675.1:g.20939G>A , LRG_476:g.20939G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397763.6:c.785G>A MANE Plus Clinical	ENSP00000380870.1:p.Gly262Asp
ENST00000300527.9:c.785G>A MANE Select	ENSP00000300527.4:p.Gly262Asp
ENST00000409416.6:c.785G>A	ENSP00000387115.1:p.Gly262Asp
ENST00000300527.8:c.785G>A	ENSP00000300527.4:p.Gly262Asp
ENST00000310645.9:c.785G>A	ENSP00000312529.5:p.Gly262Asp
ENST00000397763.5:c.785G>A	ENSP00000380870.1:p.Gly262Asp
ENST00000409416.5:c.785G>A	ENSP00000387115.1:p.Gly262Asp
ENST00000485591.1:n.441G>A
NM_001849.3:c.785G>A , LRG_476t1:c.785G>A	NP_001840.3:p.Gly262Asp
NM_058174.2:c.785G>A	NP_478054.2:p.Gly262Asp
NM_058175.2:c.785G>A	NP_478055.2:p.Gly262Asp
XM_011529451.1:c.785G>A	XP_011527753.1:p.Gly262Asp
XM_011529452.1:c.785G>A	XP_011527754.1:p.Gly262Asp
XR_937438.1:n.908G>A
XR_937439.1:n.908G>A
XR_937438.2:n.915G>A
XR_937439.2:n.915G>A
NM_001849.4:c.785G>A MANE Select	NP_001840.3:p.Gly262Asp
NM_058174.3:c.785G>A MANE Plus Clinical	NP_478054.2:p.Gly262Asp
NM_058175.3:c.785G>A	NP_478055.2:p.Gly262Asp