Canonical Allele Identifier: CA10073141

Gene: COL6A2

Linked Data

• ClinVar Variation Id: 281959
• ClinVar RCV Id: RCV000724993 ; RCV001087941
• dbSNP Id: rs61735832
• ExAC: 21:47552424 G / A
• gnomAD v2: 21-47552424-G-A
• gnomAD v3: 21-46132510-G-A
• gnomAD v4: 21-46132510-G-A
• COSMIC: COSM2822516
• MyVariant Identifiers: chr21:g.47552424G>A (hg19) ; chr21:g.46132510G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46132510G>A , CM000683.2:g.46132510G>A	GRCh38
NC_000021.8:g.47552424G>A , CM000683.1:g.47552424G>A	GRCh37
NC_000021.7:g.46376852G>A	NCBI36
NG_008675.1:g.39392G>A , LRG_476:g.39392G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300527.9:c.3018G>A MANE Select	ENSP00000300527.4:p.Ala1006=
ENST00000300527.8:c.3018G>A	ENSP00000300527.4:p.Ala1006=
NM_001849.3:c.3018G>A , LRG_476t1:c.3018G>A	NP_001840.3:p.Ala1006=
XM_011529451.1:c.3018G>A	XP_011527753.1:p.Ala1006=
XM_011529452.1:c.3018G>A	XP_011527754.1:p.Ala1006=
XR_937438.1:n.3095G>A
XR_937438.2:n.3102G>A
NM_001849.4:c.3018G>A MANE Select	NP_001840.3:p.Ala1006=