Canonical Allele Identifier: CA351201686

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238253030G>C (hg19) ; chr2:g.237344387G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344387G>C , CM000664.2:g.237344387G>C	GRCh38
NC_000002.11:g.238253030G>C , CM000664.1:g.238253030G>C	GRCh37
NC_000002.10:g.237917769G>C	NCBI36
NG_008676.1:g.74821C>G , LRG_473:g.74821C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.276C>G
ENST00000353578.9:c.7013C>G	ENSP00000315873.4:p.Thr2338Arg
ENST00000295550.9:c.7631C>G MANE Select	ENSP00000295550.4:p.Thr2544Arg
ENST00000295550.8:c.7631C>G	ENSP00000295550.4:p.Thr2544Arg
ENST00000347401.7:c.5807C>G	ENSP00000315609.4:p.Thr1936Arg
ENST00000353578.8:c.7013C>G	ENSP00000315873.4:p.Thr2338Arg
ENST00000409809.5:c.7013C>G	ENSP00000386844.1:p.Thr2338Arg
ENST00000472056.5:c.5810C>G	ENSP00000418285.1:p.Thr1937Arg
ENST00000491769.1:n.1885C>G
NM_004369.3:c.7631C>G , LRG_473t1:c.7631C>G	NP_004360.2:p.Thr2544Arg
NM_057166.4:c.5810C>G	NP_476507.3:p.Thr1937Arg
NM_057167.3:c.7013C>G	NP_476508.2:p.Thr2338Arg
XM_005246065.1:c.7031C>G	XP_005246122.1:p.Thr2344Arg
XM_005246066.1:c.6410C>G	XP_005246123.1:p.Thr2137Arg
XM_006712253.1:c.7130C>G	XP_006712316.1:p.Thr2377Arg
XM_011510574.1:c.7628C>G	XP_011508876.1:p.Thr2543Arg
XM_011510575.1:c.5225C>G	XP_011508877.1:p.Thr1742Arg
XM_017003304.1:c.5225C>G	XP_016858793.1:p.Thr1742Arg
XM_024452684.1:c.6410C>G	XP_024308452.1:p.Thr2137Arg
NM_004369.4:c.7631C>G MANE Select	NP_004360.2:p.Thr2544Arg
NM_057166.5:c.5810C>G	NP_476507.3:p.Thr1937Arg
NM_057167.4:c.7013C>G	NP_476508.2:p.Thr2338Arg