Canonical Allele Identifier: CA351191035

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238244825T>C (hg19) ; chr2:g.237336182T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336182T>C , CM000664.2:g.237336182T>C	GRCh38
NC_000002.11:g.238244825T>C , CM000664.1:g.238244825T>C	GRCh37
NC_000002.10:g.237909564T>C	NCBI36
NG_008676.1:g.83026A>G , LRG_473:g.83026A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1563A>G
ENST00000353578.9:c.8300A>G	ENSP00000315873.4:p.Gln2767Arg
ENST00000682957.1:c.1045A>G
ENST00000684508.1:n.1185A>G
ENST00000295550.9:c.8918A>G MANE Select	ENSP00000295550.4:p.Gln2973Arg
ENST00000295550.8:c.8918A>G	ENSP00000295550.4:p.Gln2973Arg
ENST00000347401.7:c.7094A>G	ENSP00000315609.4:p.Gln2365Arg
ENST00000353578.8:c.8300A>G	ENSP00000315873.4:p.Gln2767Arg
ENST00000409809.5:c.8300A>G	ENSP00000386844.1:p.Gln2767Arg
ENST00000472056.5:c.7097A>G	ENSP00000418285.1:p.Gln2366Arg
ENST00000491769.1:n.5360A>G
NM_004369.3:c.8918A>G , LRG_473t1:c.8918A>G	NP_004360.2:p.Gln2973Arg
NM_057166.4:c.7097A>G	NP_476507.3:p.Gln2366Arg
NM_057167.3:c.8300A>G	NP_476508.2:p.Gln2767Arg
XM_005246065.1:c.8318A>G	XP_005246122.1:p.Gln2773Arg
XM_005246066.1:c.7697A>G	XP_005246123.1:p.Gln2566Arg
XM_006712253.1:c.8417A>G	XP_006712316.1:p.Gln2806Arg
XM_011510574.1:c.8915A>G	XP_011508876.1:p.Gln2972Arg
XM_011510575.1:c.6512A>G	XP_011508877.1:p.Gln2171Arg
XM_017003304.1:c.6512A>G	XP_016858793.1:p.Gln2171Arg
XM_024452684.1:c.7697A>G	XP_024308452.1:p.Gln2566Arg
NM_004369.4:c.8918A>G MANE Select	NP_004360.2:p.Gln2973Arg
NM_057166.5:c.7097A>G	NP_476507.3:p.Gln2366Arg
NM_057167.4:c.8300A>G	NP_476508.2:p.Gln2767Arg