Canonical Allele Identifier: CA351216664

Gene: COL6A3

Linked Data

• ClinVar Variation Id: 2183966
• ClinVar RCV Id: RCV002627891
• MyVariant Identifiers: chr2:g.238268781C>T (hg19) ; chr2:g.237360138C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237360138C>T , CM000664.2:g.237360138C>T	GRCh38
NC_000002.11:g.238268781C>T , CM000664.1:g.238268781C>T	GRCh37
NC_000002.10:g.237933520C>T	NCBI36
NG_008676.1:g.59070G>A , LRG_473:g.59070G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000353578.9:c.5614G>A	ENSP00000315873.4:p.Val1872Met
ENST00000295550.9:c.6232G>A MANE Select	ENSP00000295550.4:p.Val2078Met
ENST00000295550.8:c.6232G>A	ENSP00000295550.4:p.Val2078Met
ENST00000347401.7:c.4411G>A	ENSP00000315609.4:p.Val1471Met
ENST00000353578.8:c.5614G>A	ENSP00000315873.4:p.Val1872Met
ENST00000409809.5:c.5614G>A	ENSP00000386844.1:p.Val1872Met
ENST00000472056.5:c.4411G>A	ENSP00000418285.1:p.Val1471Met
NM_004369.3:c.6232G>A , LRG_473t1:c.6232G>A	NP_004360.2:p.Val2078Met
NM_057166.4:c.4411G>A	NP_476507.3:p.Val1471Met
NM_057167.3:c.5614G>A	NP_476508.2:p.Val1872Met
XM_005246065.1:c.5632G>A	XP_005246122.1:p.Val1878Met
XM_005246066.1:c.5011G>A	XP_005246123.1:p.Val1671Met
XM_006712253.1:c.5731G>A	XP_006712316.1:p.Val1911Met
XM_011510574.1:c.6229G>A	XP_011508876.1:p.Val2077Met
XM_011510575.1:c.3826G>A	XP_011508877.1:p.Val1276Met
XM_017003304.1:c.3826G>A	XP_016858793.1:p.Val1276Met
XM_024452684.1:c.5011G>A	XP_024308452.1:p.Val1671Met
NM_004369.4:c.6232G>A MANE Select	NP_004360.2:p.Val2078Met
NM_057166.5:c.4411G>A	NP_476507.3:p.Val1471Met
NM_057167.4:c.5614G>A	NP_476508.2:p.Val1872Met