Canonical Allele Identifier: CA431701783

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238244968T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336325T>A , CM000664.2:g.237336325T>A	GRCh38
NC_000002.11:g.238244968T>A , CM000664.1:g.238244968T>A	GRCh37
NC_000002.10:g.237909707T>A	NCBI36
NG_008676.1:g.82883A>T , LRG_473:g.82883A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1420A>T
ENST00000353578.9:c.8157A>T	ENSP00000315873.4:p.Thr2719=
ENST00000682957.1:c.902A>T
ENST00000684508.1:n.1042A>T
ENST00000295550.9:c.8775A>T MANE Select	ENSP00000295550.4:p.Thr2925=
ENST00000295550.8:c.8775A>T	ENSP00000295550.4:p.Thr2925=
ENST00000347401.7:c.6951A>T	ENSP00000315609.4:p.Thr2317=
ENST00000353578.8:c.8157A>T	ENSP00000315873.4:p.Thr2719=
ENST00000409809.5:c.8157A>T	ENSP00000386844.1:p.Thr2719=
ENST00000472056.5:c.6954A>T	ENSP00000418285.1:p.Thr2318=
ENST00000491769.1:n.5217A>T
NM_004369.3:c.8775A>T , LRG_473t1:c.8775A>T	NP_004360.2:p.Thr2925=
NM_057166.4:c.6954A>T	NP_476507.3:p.Thr2318=
NM_057167.3:c.8157A>T	NP_476508.2:p.Thr2719=
XM_005246065.1:c.8175A>T	XP_005246122.1:p.Thr2725=
XM_005246066.1:c.7554A>T	XP_005246123.1:p.Thr2518=
XM_006712253.1:c.8274A>T	XP_006712316.1:p.Thr2758=
XM_011510574.1:c.8772A>T	XP_011508876.1:p.Thr2924=
XM_011510575.1:c.6369A>T	XP_011508877.1:p.Thr2123=
XM_017003304.1:c.6369A>T	XP_016858793.1:p.Thr2123=
XM_024452684.1:c.7554A>T	XP_024308452.1:p.Thr2518=
NM_004369.4:c.8775A>T MANE Select	NP_004360.2:p.Thr2925=
NM_057166.5:c.6954A>T	NP_476507.3:p.Thr2318=
NM_057167.4:c.8157A>T	NP_476508.2:p.Thr2719=