Canonical Allele Identifier: CA658657258

Gene: COL6A3

Linked Data

• ClinVar Variation Id: 449325
• ClinVar RCV Id: RCV000521476 ; RCV001809468
• dbSNP Id: rs1553553327
• MyVariant Identifiers: chr2:g.238268002T>C (hg19) ; chr2:g.237359359T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237359359T>C , CM000664.2:g.237359359T>C	GRCh38
NC_000002.11:g.238268002T>C , CM000664.1:g.238268002T>C	GRCh37
NC_000002.10:g.237932741T>C	NCBI36
NG_008676.1:g.59849A>G , LRG_473:g.59849A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353578.9:c.5691+3A>G	ENSP00000315873.4:n.5691+3A>G
ENST00000295550.9:c.6309+3A>G MANE Select	ENSP00000295550.4:n.6309+3A>G
ENST00000295550.8:c.6309+3A>G	ENSP00000295550.4:n.6309+3A>G
ENST00000347401.7:c.4488+3A>G	ENSP00000315609.4:n.4488+3A>G
ENST00000353578.8:c.5691+3A>G	ENSP00000315873.4:n.5691+3A>G
ENST00000409809.5:c.5691+3A>G	ENSP00000386844.1:n.5691+3A>G
ENST00000472056.5:c.4488+3A>G	ENSP00000418285.1:n.4488+3A>G
NM_004369.3:c.6309+3A>G , LRG_473t1:c.6309+3A>G	NP_004360.2:n.6309+3A>G
NM_057166.4:c.4488+3A>G	NP_476507.3:n.4488+3A>G
NM_057167.3:c.5691+3A>G	NP_476508.2:n.5691+3A>G
XM_005246065.1:c.5709+3A>G	XP_005246122.1:n.5709+3A>G
XM_005246066.1:c.5088+3A>G	XP_005246123.1:n.5088+3A>G
XM_006712253.1:c.5808+3A>G	XP_006712316.1:n.5808+3A>G
XM_011510574.1:c.6306+3A>G	XP_011508876.1:n.6306+3A>G
XM_011510575.1:c.3903+3A>G	XP_011508877.1:n.3903+3A>G
XM_017003304.1:c.3903+3A>G	XP_016858793.1:n.3903+3A>G
XM_024452684.1:c.5088+3A>G	XP_024308452.1:n.5088+3A>G
NM_004369.4:c.6309+3A>G MANE Select	NP_004360.2:n.6309+3A>G
NM_057166.5:c.4488+3A>G	NP_476507.3:n.4488+3A>G
NM_057167.4:c.5691+3A>G	NP_476508.2:n.5691+3A>G