Canonical Allele Identifier: CA410524952

Gene: COL6A2

Linked Data

• ClinVar Variation Id: 444578
• ClinVar RCV Id: RCV000513339 ; RCV001857321
• dbSNP Id: rs1057517988
• MyVariant Identifiers: chr21:g.47535840G>C (hg19) ; chr21:g.46115926G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.46115926G>C , CM000683.2:g.46115926G>C	GRCh38
NC_000021.8:g.47535840G>C , CM000683.1:g.47535840G>C	GRCh37
NC_000021.7:g.46360268G>C	NCBI36
NG_008675.1:g.22808G>C , LRG_476:g.22808G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000397763.6:c.855+1G>C MANE Plus Clinical	ENSP00000380870.1:n.855+1G>C
ENST00000300527.9:c.855+1G>C MANE Select	ENSP00000300527.4:n.855+1G>C
ENST00000409416.6:c.855+1G>C	ENSP00000387115.1:n.855+1G>C
ENST00000300527.8:c.855+1G>C	ENSP00000300527.4:n.855+1G>C
ENST00000310645.9:c.855+1G>C	ENSP00000312529.5:n.855+1G>C
ENST00000397763.5:c.855+1G>C	ENSP00000380870.1:n.855+1G>C
ENST00000409416.5:c.855+1G>C	ENSP00000387115.1:n.855+1G>C
ENST00000485591.1:n.511+1G>C
NM_001849.3:c.855+1G>C , LRG_476t1:c.855+1G>C	NP_001840.3:n.855+1G>C
NM_058174.2:c.855+1G>C	NP_478054.2:n.855+1G>C
NM_058175.2:c.855+1G>C	NP_478055.2:n.855+1G>C
XM_011529451.1:c.855+1G>C	XP_011527753.1:n.855+1G>C
XM_011529452.1:c.855+1G>C	XP_011527754.1:n.855+1G>C
XR_937438.1:n.978+1G>C
XR_937439.1:n.978+1G>C
XR_937438.2:n.985+1G>C
XR_937439.2:n.985+1G>C
NM_001849.4:c.855+1G>C MANE Select	NP_001840.3:n.855+1G>C
NM_058174.3:c.855+1G>C MANE Plus Clinical	NP_478054.2:n.855+1G>C
NM_058175.3:c.855+1G>C	NP_478055.2:n.855+1G>C