Canonical Allele Identifier: CA351191970

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238245122G>C (hg19) ; chr2:g.237336479G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336479G>C , CM000664.2:g.237336479G>C	GRCh38
NC_000002.11:g.238245122G>C , CM000664.1:g.238245122G>C	GRCh37
NC_000002.10:g.237909861G>C	NCBI36
NG_008676.1:g.82729C>G , LRG_473:g.82729C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1266C>G
ENST00000353578.9:c.8003C>G	ENSP00000315873.4:p.Thr2668Arg
ENST00000682957.1:c.748C>G
ENST00000684508.1:n.888C>G
ENST00000295550.9:c.8621C>G MANE Select	ENSP00000295550.4:p.Thr2874Arg
ENST00000295550.8:c.8621C>G	ENSP00000295550.4:p.Thr2874Arg
ENST00000347401.7:c.6797C>G	ENSP00000315609.4:p.Thr2266Arg
ENST00000353578.8:c.8003C>G	ENSP00000315873.4:p.Thr2668Arg
ENST00000409809.5:c.8003C>G	ENSP00000386844.1:p.Thr2668Arg
ENST00000472056.5:c.6800C>G	ENSP00000418285.1:p.Thr2267Arg
ENST00000491769.1:n.5063C>G
NM_004369.3:c.8621C>G , LRG_473t1:c.8621C>G	NP_004360.2:p.Thr2874Arg
NM_057166.4:c.6800C>G	NP_476507.3:p.Thr2267Arg
NM_057167.3:c.8003C>G	NP_476508.2:p.Thr2668Arg
XM_005246065.1:c.8021C>G	XP_005246122.1:p.Thr2674Arg
XM_005246066.1:c.7400C>G	XP_005246123.1:p.Thr2467Arg
XM_006712253.1:c.8120C>G	XP_006712316.1:p.Thr2707Arg
XM_011510574.1:c.8618C>G	XP_011508876.1:p.Thr2873Arg
XM_011510575.1:c.6215C>G	XP_011508877.1:p.Thr2072Arg
XM_017003304.1:c.6215C>G	XP_016858793.1:p.Thr2072Arg
XM_024452684.1:c.7400C>G	XP_024308452.1:p.Thr2467Arg
NM_004369.4:c.8621C>G MANE Select	NP_004360.2:p.Thr2874Arg
NM_057166.5:c.6800C>G	NP_476507.3:p.Thr2267Arg
NM_057167.4:c.8003C>G	NP_476508.2:p.Thr2668Arg