Canonical Allele Identifier: CA351191919

Gene: COL6A3

Linked Data

• dbSNP Id: rs1574932113
• MyVariant Identifiers: chr2:g.238245093T>G (hg19) ; chr2:g.237336450T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336450T>G , CM000664.2:g.237336450T>G	GRCh38
NC_000002.11:g.238245093T>G , CM000664.1:g.238245093T>G	GRCh37
NC_000002.10:g.237909832T>G	NCBI36
NG_008676.1:g.82758A>C , LRG_473:g.82758A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1295A>C
ENST00000353578.9:c.8032A>C	ENSP00000315873.4:p.Thr2678Pro
ENST00000682957.1:c.777A>C
ENST00000684508.1:n.917A>C
ENST00000295550.9:c.8650A>C MANE Select	ENSP00000295550.4:p.Thr2884Pro
ENST00000295550.8:c.8650A>C	ENSP00000295550.4:p.Thr2884Pro
ENST00000347401.7:c.6826A>C	ENSP00000315609.4:p.Thr2276Pro
ENST00000353578.8:c.8032A>C	ENSP00000315873.4:p.Thr2678Pro
ENST00000409809.5:c.8032A>C	ENSP00000386844.1:p.Thr2678Pro
ENST00000472056.5:c.6829A>C	ENSP00000418285.1:p.Thr2277Pro
ENST00000491769.1:n.5092A>C
NM_004369.3:c.8650A>C , LRG_473t1:c.8650A>C	NP_004360.2:p.Thr2884Pro
NM_057166.4:c.6829A>C	NP_476507.3:p.Thr2277Pro
NM_057167.3:c.8032A>C	NP_476508.2:p.Thr2678Pro
XM_005246065.1:c.8050A>C	XP_005246122.1:p.Thr2684Pro
XM_005246066.1:c.7429A>C	XP_005246123.1:p.Thr2477Pro
XM_006712253.1:c.8149A>C	XP_006712316.1:p.Thr2717Pro
XM_011510574.1:c.8647A>C	XP_011508876.1:p.Thr2883Pro
XM_011510575.1:c.6244A>C	XP_011508877.1:p.Thr2082Pro
XM_017003304.1:c.6244A>C	XP_016858793.1:p.Thr2082Pro
XM_024452684.1:c.7429A>C	XP_024308452.1:p.Thr2477Pro
NM_004369.4:c.8650A>C MANE Select	NP_004360.2:p.Thr2884Pro
NM_057166.5:c.6829A>C	NP_476507.3:p.Thr2277Pro
NM_057167.4:c.8032A>C	NP_476508.2:p.Thr2678Pro