Canonical Allele Identifier: CA67830327

Gene: COL6A3

Linked Data

• dbSNP Id: rs537725110
• gnomAD v3: 2-237336163-G-A
• gnomAD v4: 2-237336163-G-A
• MyVariant Identifiers: chr2:g.238244806G>A (hg19) ; chr2:g.237336163G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336163G>A , CM000664.2:g.237336163G>A	GRCh38
NC_000002.11:g.238244806G>A , CM000664.1:g.238244806G>A	GRCh37
NC_000002.10:g.237909545G>A	NCBI36
NG_008676.1:g.83045C>T , LRG_473:g.83045C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1582C>T
ENST00000353578.9:c.8319C>T	ENSP00000315873.4:p.Ala2773=
ENST00000682957.1:c.1064C>T
ENST00000684508.1:n.1204C>T
ENST00000295550.9:c.8937C>T MANE Select	ENSP00000295550.4:p.Ala2979=
ENST00000295550.8:c.8937C>T	ENSP00000295550.4:p.Ala2979=
ENST00000347401.7:c.7113C>T	ENSP00000315609.4:p.Ala2371=
ENST00000353578.8:c.8319C>T	ENSP00000315873.4:p.Ala2773=
ENST00000409809.5:c.8319C>T	ENSP00000386844.1:p.Ala2773=
ENST00000472056.5:c.7116C>T	ENSP00000418285.1:p.Ala2372=
ENST00000491769.1:n.5379C>T
NM_004369.3:c.8937C>T , LRG_473t1:c.8937C>T	NP_004360.2:p.Ala2979=
NM_057166.4:c.7116C>T	NP_476507.3:p.Ala2372=
NM_057167.3:c.8319C>T	NP_476508.2:p.Ala2773=
XM_005246065.1:c.8337C>T	XP_005246122.1:p.Ala2779=
XM_005246066.1:c.7716C>T	XP_005246123.1:p.Ala2572=
XM_006712253.1:c.8436C>T	XP_006712316.1:p.Ala2812=
XM_011510574.1:c.8934C>T	XP_011508876.1:p.Ala2978=
XM_011510575.1:c.6531C>T	XP_011508877.1:p.Ala2177=
XM_017003304.1:c.6531C>T	XP_016858793.1:p.Ala2177=
XM_024452684.1:c.7716C>T	XP_024308452.1:p.Ala2572=
NM_004369.4:c.8937C>T MANE Select	NP_004360.2:p.Ala2979=
NM_057166.5:c.7116C>T	NP_476507.3:p.Ala2372=
NM_057167.4:c.8319C>T	NP_476508.2:p.Ala2773=