Canonical Allele Identifier: CA2189266
Gene: COL6A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 288419
dbSNP Id: rs370664069

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.237376787C>T , CM000664.2:g.237376787C>T GRCh38
NC_000002.11:g.238285430C>T , CM000664.1:g.238285430C>T GRCh37
NC_000002.10:g.237950169C>T NCBI36
NG_008676.1:g.42421G>A , LRG_473:g.42421G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000353578.9:c.2437G>A ENSP00000315873.4:p.Gly813Arg
ENST00000295550.9:c.3055G>A MANE Select ENSP00000295550.4:p.Gly1019Arg
ENST00000295550.8:c.3055G>A ENSP00000295550.4:p.Gly1019Arg
ENST00000347401.7:c.1234G>A ENSP00000315609.4:p.Gly412Arg
ENST00000353578.8:c.2437G>A ENSP00000315873.4:p.Gly813Arg
ENST00000392003.6:c.1834G>A ENSP00000375860.2:p.Gly612Arg
ENST00000392004.7:c.2437G>A ENSP00000375861.3:p.Gly813Arg
ENST00000409809.5:c.2437G>A ENSP00000386844.1:p.Gly813Arg
ENST00000472056.5:c.1234G>A ENSP00000418285.1:p.Gly412Arg
NM_004369.3:c.3055G>A , LRG_473t1:c.3055G>A NP_004360.2:p.Gly1019Arg
NM_057164.4:c.1834G>A NP_476505.3:p.Gly612Arg
NM_057165.4:c.2437G>A NP_476506.3:p.Gly813Arg
NM_057166.4:c.1234G>A NP_476507.3:p.Gly412Arg
NM_057167.3:c.2437G>A NP_476508.2:p.Gly813Arg
XM_005246065.1:c.2455G>A XP_005246122.1:p.Gly819Arg
XM_005246066.1:c.1834G>A XP_005246123.1:p.Gly612Arg
XM_006712253.1:c.3055G>A XP_006712316.1:p.Gly1019Arg
XM_011510574.1:c.3055G>A XP_011508876.1:p.Gly1019Arg
XM_011510575.1:c.649G>A XP_011508877.1:p.Gly217Arg
XM_017003304.1:c.649G>A XP_016858793.1:p.Gly217Arg
XM_024452684.1:c.1834G>A XP_024308452.1:p.Gly612Arg
NM_004369.4:c.3055G>A MANE Select NP_004360.2:p.Gly1019Arg
NM_057164.5:c.1834G>A NP_476505.3:p.Gly612Arg
NM_057165.5:c.2437G>A NP_476506.3:p.Gly813Arg
NM_057166.5:c.1234G>A NP_476507.3:p.Gly412Arg
NM_057167.4:c.2437G>A NP_476508.2:p.Gly813Arg