Canonical Allele Identifier: CA351216634

Gene: COL6A3

Linked Data

• ClinVar Variation Id: 520883
• ClinVar RCV Id: RCV000623881 ; RCV001860425
• dbSNP Id: rs1553553625
• MyVariant Identifiers: chr2:g.238268775C>G (hg19) ; chr2:g.237360132C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237360132C>G , CM000664.2:g.237360132C>G	GRCh38
NC_000002.11:g.238268775C>G , CM000664.1:g.238268775C>G	GRCh37
NC_000002.10:g.237933514C>G	NCBI36
NG_008676.1:g.59076G>C , LRG_473:g.59076G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353578.9:c.5620G>C	ENSP00000315873.4:p.Gly1874Arg
ENST00000295550.9:c.6238G>C MANE Select	ENSP00000295550.4:p.Gly2080Arg
ENST00000295550.8:c.6238G>C	ENSP00000295550.4:p.Gly2080Arg
ENST00000347401.7:c.4417G>C	ENSP00000315609.4:p.Gly1473Arg
ENST00000353578.8:c.5620G>C	ENSP00000315873.4:p.Gly1874Arg
ENST00000409809.5:c.5620G>C	ENSP00000386844.1:p.Gly1874Arg
ENST00000472056.5:c.4417G>C	ENSP00000418285.1:p.Gly1473Arg
NM_004369.3:c.6238G>C , LRG_473t1:c.6238G>C	NP_004360.2:p.Gly2080Arg
NM_057166.4:c.4417G>C	NP_476507.3:p.Gly1473Arg
NM_057167.3:c.5620G>C	NP_476508.2:p.Gly1874Arg
XM_005246065.1:c.5638G>C	XP_005246122.1:p.Gly1880Arg
XM_005246066.1:c.5017G>C	XP_005246123.1:p.Gly1673Arg
XM_006712253.1:c.5737G>C	XP_006712316.1:p.Gly1913Arg
XM_011510574.1:c.6235G>C	XP_011508876.1:p.Gly2079Arg
XM_011510575.1:c.3832G>C	XP_011508877.1:p.Gly1278Arg
XM_017003304.1:c.3832G>C	XP_016858793.1:p.Gly1278Arg
XM_024452684.1:c.5017G>C	XP_024308452.1:p.Gly1673Arg
NM_004369.4:c.6238G>C MANE Select	NP_004360.2:p.Gly2080Arg
NM_057166.5:c.4417G>C	NP_476507.3:p.Gly1473Arg
NM_057167.4:c.5620G>C	NP_476508.2:p.Gly1874Arg