Canonical Allele Identifier: CA351202793

Gene: COL6A3

Linked Data

• ClinVar Variation Id: 2440479
• ClinVar RCV Id: RCV003143313
• MyVariant Identifiers: chr2:g.238253192G>A (hg19) ; chr2:g.237344549G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344549G>A , CM000664.2:g.237344549G>A	GRCh38
NC_000002.11:g.238253192G>A , CM000664.1:g.238253192G>A	GRCh37
NC_000002.10:g.237917931G>A	NCBI36
NG_008676.1:g.74659C>T , LRG_473:g.74659C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.114C>T
ENST00000353578.9:c.6851C>T	ENSP00000315873.4:p.Ala2284Val
ENST00000295550.9:c.7469C>T MANE Select	ENSP00000295550.4:p.Ala2490Val
ENST00000295550.8:c.7469C>T	ENSP00000295550.4:p.Ala2490Val
ENST00000347401.7:c.5645C>T	ENSP00000315609.4:p.Ala1882Val
ENST00000353578.8:c.6851C>T	ENSP00000315873.4:p.Ala2284Val
ENST00000409809.5:c.6851C>T	ENSP00000386844.1:p.Ala2284Val
ENST00000472056.5:c.5648C>T	ENSP00000418285.1:p.Ala1883Val
ENST00000491769.1:n.1723C>T
NM_004369.3:c.7469C>T , LRG_473t1:c.7469C>T	NP_004360.2:p.Ala2490Val
NM_057166.4:c.5648C>T	NP_476507.3:p.Ala1883Val
NM_057167.3:c.6851C>T	NP_476508.2:p.Ala2284Val
XM_005246065.1:c.6869C>T	XP_005246122.1:p.Ala2290Val
XM_005246066.1:c.6248C>T	XP_005246123.1:p.Ala2083Val
XM_006712253.1:c.6968C>T	XP_006712316.1:p.Ala2323Val
XM_011510574.1:c.7466C>T	XP_011508876.1:p.Ala2489Val
XM_011510575.1:c.5063C>T	XP_011508877.1:p.Ala1688Val
XM_017003304.1:c.5063C>T	XP_016858793.1:p.Ala1688Val
XM_024452684.1:c.6248C>T	XP_024308452.1:p.Ala2083Val
NM_004369.4:c.7469C>T MANE Select	NP_004360.2:p.Ala2490Val
NM_057166.5:c.5648C>T	NP_476507.3:p.Ala1883Val
NM_057167.4:c.6851C>T	NP_476508.2:p.Ala2284Val