Canonical Allele Identifier: CA147502

Gene: COL6A2

Linked Data

• ClinVar Variation Id: 93953
• ClinVar RCV Id: RCV002483139
• dbSNP Id: rs141703710
• ExAC: 21:47532093 G / A
• gnomAD v2: 21-47532093-G-A
• gnomAD v3: 21-46112179-G-A
• gnomAD v4: 21-46112179-G-A
• MyVariant Identifiers: chr21:g.47532093G>A (hg19) ; chr21:g.46112179G>A (hg38)
• PubMed: PMID:15689448

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46112179G>A , CM000683.2:g.46112179G>A	GRCh38
NC_000021.8:g.47532093G>A , CM000683.1:g.47532093G>A	GRCh37
NC_000021.7:g.46356521G>A	NCBI36
NG_008675.1:g.19061G>A , LRG_476:g.19061G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000397763.6:c.316G>A MANE Plus Clinical	ENSP00000380870.1:p.Glu106Lys
ENST00000300527.9:c.316G>A MANE Select	ENSP00000300527.4:p.Glu106Lys
ENST00000409416.6:c.316G>A	ENSP00000387115.1:p.Glu106Lys
ENST00000300527.8:c.316G>A	ENSP00000300527.4:p.Glu106Lys
ENST00000310645.9:c.316G>A	ENSP00000312529.5:p.Glu106Lys
ENST00000397763.5:c.316G>A	ENSP00000380870.1:p.Glu106Lys
ENST00000409416.5:c.316G>A	ENSP00000387115.1:p.Glu106Lys
ENST00000436769.5:c.316G>A	ENSP00000390418.1:p.Glu106Lys
NM_001849.3:c.316G>A , LRG_476t1:c.316G>A	NP_001840.3:p.Glu106Lys
NM_058174.2:c.316G>A	NP_478054.2:p.Glu106Lys
NM_058175.2:c.316G>A	NP_478055.2:p.Glu106Lys
XM_011529451.1:c.316G>A	XP_011527753.1:p.Glu106Lys
XM_011529452.1:c.316G>A	XP_011527754.1:p.Glu106Lys
XR_937438.1:n.439G>A
XR_937439.1:n.439G>A
XR_937438.2:n.446G>A
XR_937439.2:n.446G>A
NM_001849.4:c.316G>A MANE Select	NP_001840.3:p.Glu106Lys
NM_058174.3:c.316G>A MANE Plus Clinical	NP_478054.2:p.Glu106Lys
NM_058175.3:c.316G>A	NP_478055.2:p.Glu106Lys