Canonical Allele Identifier: CA10605654

Gene: COL6A3

Linked Data

• ClinVar Variation Id: 287031
• ClinVar RCV Id: RCV000320923 ; RCV003631110
• dbSNP Id: rs886043555
• gnomAD v4: 2-237324819-G-A
• MyVariant Identifiers: chr2:g.238233462G>A (hg19) ; chr2:g.237324819G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237324819G>A , CM000664.2:g.237324819G>A	GRCh38
NC_000002.11:g.238233462G>A , CM000664.1:g.238233462G>A	GRCh37
NC_000002.10:g.237898201G>A	NCBI36
NG_008676.1:g.94389C>T , LRG_473:g.94389C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1875-5C>T
ENST00000353578.9:c.8876-5C>T	ENSP00000315873.4:n.8876-5C>T
ENST00000682957.1:c.1621-5C>T
ENST00000683348.1:c.360-5C>T	ENSP00000508058.1:n.360-5C>T
ENST00000295550.9:c.9494-5C>T MANE Select	ENSP00000295550.4:n.9494-5C>T
ENST00000295550.8:c.9494-5C>T	ENSP00000295550.4:n.9494-5C>T
ENST00000347401.7:c.7670-5C>T	ENSP00000315609.4:n.7670-5C>T
ENST00000353578.8:c.8876-5C>T	ENSP00000315873.4:n.8876-5C>T
ENST00000409809.5:c.8876-5C>T	ENSP00000386844.1:n.8876-5C>T
ENST00000472056.5:c.7673-5C>T	ENSP00000418285.1:n.7673-5C>T
ENST00000473258.1:n.4622-5C>T
ENST00000491769.1:n.5936-5C>T
NM_004369.3:c.9494-5C>T , LRG_473t1:c.9494-5C>T	NP_004360.2:n.9494-5C>T
NM_057166.4:c.7673-5C>T	NP_476507.3:n.7673-5C>T
NM_057167.3:c.8876-5C>T	NP_476508.2:n.8876-5C>T
XM_005246065.1:c.8894-5C>T	XP_005246122.1:n.8894-5C>T
XM_005246066.1:c.8273-5C>T	XP_005246123.1:n.8273-5C>T
XM_006712253.1:c.8993-5C>T	XP_006712316.1:n.8993-5C>T
XM_011510574.1:c.9491-5C>T	XP_011508876.1:n.9491-5C>T
XM_011510575.1:c.7088-5C>T	XP_011508877.1:n.7088-5C>T
XM_017003304.1:c.7088-5C>T	XP_016858793.1:n.7088-5C>T
XM_024452684.1:c.8273-5C>T	XP_024308452.1:n.8273-5C>T
NM_004369.4:c.9494-5C>T MANE Select	NP_004360.2:n.9494-5C>T
NM_057166.5:c.7673-5C>T	NP_476507.3:n.7673-5C>T
NM_057167.4:c.8876-5C>T	NP_476508.2:n.8876-5C>T