Canonical Allele Identifier: CA295320

Gene: COL6A3

Linked Data

• ClinVar Variation Id: 2726290
• ClinVar RCV Id: RCV003518515
• dbSNP Id: rs727502837
• ExAC: 2:238244823 C / T
• gnomAD v2: 2-238244823-C-T
• gnomAD v3: 2-237336180-C-T
• gnomAD v4: 2-237336180-C-T
• MyVariant Identifiers: chr2:g.238244823C>T (hg19) ; chr2:g.237336180C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336180C>T , CM000664.2:g.237336180C>T	GRCh38
NC_000002.11:g.238244823C>T , CM000664.1:g.238244823C>T	GRCh37
NC_000002.10:g.237909562C>T	NCBI36
NG_008676.1:g.83028G>A , LRG_473:g.83028G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1565G>A
ENST00000353578.9:c.8302G>A	ENSP00000315873.4:p.Ala2768Thr
ENST00000682957.1:c.1047G>A
ENST00000684508.1:n.1187G>A
ENST00000295550.9:c.8920G>A MANE Select	ENSP00000295550.4:p.Ala2974Thr
ENST00000295550.8:c.8920G>A	ENSP00000295550.4:p.Ala2974Thr
ENST00000347401.7:c.7096G>A	ENSP00000315609.4:p.Ala2366Thr
ENST00000353578.8:c.8302G>A	ENSP00000315873.4:p.Ala2768Thr
ENST00000409809.5:c.8302G>A	ENSP00000386844.1:p.Ala2768Thr
ENST00000472056.5:c.7099G>A	ENSP00000418285.1:p.Ala2367Thr
ENST00000491769.1:n.5362G>A
NM_004369.3:c.8920G>A , LRG_473t1:c.8920G>A	NP_004360.2:p.Ala2974Thr
NM_057166.4:c.7099G>A	NP_476507.3:p.Ala2367Thr
NM_057167.3:c.8302G>A	NP_476508.2:p.Ala2768Thr
XM_005246065.1:c.8320G>A	XP_005246122.1:p.Ala2774Thr
XM_005246066.1:c.7699G>A	XP_005246123.1:p.Ala2567Thr
XM_006712253.1:c.8419G>A	XP_006712316.1:p.Ala2807Thr
XM_011510574.1:c.8917G>A	XP_011508876.1:p.Ala2973Thr
XM_011510575.1:c.6514G>A	XP_011508877.1:p.Ala2172Thr
XM_017003304.1:c.6514G>A	XP_016858793.1:p.Ala2172Thr
XM_024452684.1:c.7699G>A	XP_024308452.1:p.Ala2567Thr
NM_004369.4:c.8920G>A MANE Select	NP_004360.2:p.Ala2974Thr
NM_057166.5:c.7099G>A	NP_476507.3:p.Ala2367Thr
NM_057167.4:c.8302G>A	NP_476508.2:p.Ala2768Thr