Canonical Allele Identifier: CA410527294

Gene: COL6A2

Linked Data

• ClinVar Variation Id: 476446
• ClinVar RCV Id: RCV000540933 ; RCV000578736
• dbSNP Id: rs1555873356
• MyVariant Identifiers: chr21:g.47537312A>C (hg19) ; chr21:g.46117398A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46117398A>C , CM000683.2:g.46117398A>C	GRCh38
NC_000021.8:g.47537312A>C , CM000683.1:g.47537312A>C	GRCh37
NC_000021.7:g.46361740A>C	NCBI36
NG_008675.1:g.24280A>C , LRG_476:g.24280A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397763.6:c.1000-2A>C MANE Plus Clinical	ENSP00000380870.1:n.1000-2A>C
ENST00000300527.9:c.1000-2A>C MANE Select	ENSP00000300527.4:n.1000-2A>C
ENST00000409416.6:c.1000-2A>C	ENSP00000387115.1:n.1000-2A>C
ENST00000300527.8:c.1000-2A>C	ENSP00000300527.4:n.1000-2A>C
ENST00000310645.9:c.1000-2A>C	ENSP00000312529.5:n.1000-2A>C
ENST00000397763.5:c.1000-2A>C	ENSP00000380870.1:n.1000-2A>C
ENST00000409416.5:c.1000-2A>C	ENSP00000387115.1:n.1000-2A>C
ENST00000485591.1:n.656-2A>C
NM_001849.3:c.1000-2A>C , LRG_476t1:c.1000-2A>C	NP_001840.3:n.1000-2A>C
NM_058174.2:c.1000-2A>C	NP_478054.2:n.1000-2A>C
NM_058175.2:c.1000-2A>C	NP_478055.2:n.1000-2A>C
XM_011529451.1:c.1000-2A>C	XP_011527753.1:n.1000-2A>C
XM_011529452.1:c.1000-2A>C	XP_011527754.1:n.1000-2A>C
XR_937438.1:n.1123-2A>C
XR_937439.1:n.1123-2A>C
XR_937438.2:n.1130-2A>C
XR_937439.2:n.1130-2A>C
NM_001849.4:c.1000-2A>C MANE Select	NP_001840.3:n.1000-2A>C
NM_058174.3:c.1000-2A>C MANE Plus Clinical	NP_478054.2:n.1000-2A>C
NM_058175.3:c.1000-2A>C	NP_478055.2:n.1000-2A>C