Canonical Allele Identifier: CA410538362

Gene: COL6A2

Linked Data

• ClinVar Variation Id: 2269596
• ClinVar RCV Id: RCV002799435
• gnomAD v4: 21-46125468-G-A
• MyVariant Identifiers: chr21:g.47545382G>A (hg19) ; chr21:g.46125468G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46125468G>A , CM000683.2:g.46125468G>A	GRCh38
NC_000021.8:g.47545382G>A , CM000683.1:g.47545382G>A	GRCh37
NC_000021.7:g.46369810G>A	NCBI36
NG_008675.1:g.32350G>A , LRG_476:g.32350G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397763.6:c.1820G>A MANE Plus Clinical	ENSP00000380870.1:p.Cys607Tyr
ENST00000300527.9:c.1820G>A MANE Select	ENSP00000300527.4:p.Cys607Tyr
ENST00000409416.6:c.1820G>A	ENSP00000387115.1:p.Cys607Tyr
ENST00000300527.8:c.1820G>A	ENSP00000300527.4:p.Cys607Tyr
ENST00000310645.9:c.1820G>A	ENSP00000312529.5:p.Cys607Tyr
ENST00000397763.5:c.1820G>A	ENSP00000380870.1:p.Cys607Tyr
ENST00000409416.5:c.1820G>A	ENSP00000387115.1:p.Cys607Tyr
ENST00000413758.1:c.491G>A	ENSP00000395751.1:p.Cys164Tyr
NM_001849.3:c.1820G>A , LRG_476t1:c.1820G>A	NP_001840.3:p.Cys607Tyr
NM_058174.2:c.1820G>A	NP_478054.2:p.Cys607Tyr
NM_058175.2:c.1820G>A	NP_478055.2:p.Cys607Tyr
XM_011529451.1:c.1820G>A	XP_011527753.1:p.Cys607Tyr
XM_011529452.1:c.1820G>A	XP_011527754.1:p.Cys607Tyr
XR_937438.1:n.1897G>A
XR_937439.1:n.1897G>A
XR_937438.2:n.1904G>A
XR_937439.2:n.1904G>A
NM_001849.4:c.1820G>A MANE Select	NP_001840.3:p.Cys607Tyr
NM_058174.3:c.1820G>A MANE Plus Clinical	NP_478054.2:p.Cys607Tyr
NM_058175.3:c.1820G>A	NP_478055.2:p.Cys607Tyr