Canonical Allele Identifier: CA351191286

Gene: COL6A3

Linked Data

• MyVariant Identifiers: chr2:g.238244903G>C (hg19) ; chr2:g.237336260G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336260G>C , CM000664.2:g.237336260G>C	GRCh38
NC_000002.11:g.238244903G>C , CM000664.1:g.238244903G>C	GRCh37
NC_000002.10:g.237909642G>C	NCBI36
NG_008676.1:g.82948C>G , LRG_473:g.82948C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000347401.8:c.1485C>G
ENST00000353578.9:c.8222C>G	ENSP00000315873.4:p.Ala2741Gly
ENST00000682957.1:c.967C>G
ENST00000684508.1:n.1107C>G
ENST00000295550.9:c.8840C>G MANE Select	ENSP00000295550.4:p.Ala2947Gly
ENST00000295550.8:c.8840C>G	ENSP00000295550.4:p.Ala2947Gly
ENST00000347401.7:c.7016C>G	ENSP00000315609.4:p.Ala2339Gly
ENST00000353578.8:c.8222C>G	ENSP00000315873.4:p.Ala2741Gly
ENST00000409809.5:c.8222C>G	ENSP00000386844.1:p.Ala2741Gly
ENST00000472056.5:c.7019C>G	ENSP00000418285.1:p.Ala2340Gly
ENST00000491769.1:n.5282C>G
NM_004369.3:c.8840C>G , LRG_473t1:c.8840C>G	NP_004360.2:p.Ala2947Gly
NM_057166.4:c.7019C>G	NP_476507.3:p.Ala2340Gly
NM_057167.3:c.8222C>G	NP_476508.2:p.Ala2741Gly
XM_005246065.1:c.8240C>G	XP_005246122.1:p.Ala2747Gly
XM_005246066.1:c.7619C>G	XP_005246123.1:p.Ala2540Gly
XM_006712253.1:c.8339C>G	XP_006712316.1:p.Ala2780Gly
XM_011510574.1:c.8837C>G	XP_011508876.1:p.Ala2946Gly
XM_011510575.1:c.6434C>G	XP_011508877.1:p.Ala2145Gly
XM_017003304.1:c.6434C>G	XP_016858793.1:p.Ala2145Gly
XM_024452684.1:c.7619C>G	XP_024308452.1:p.Ala2540Gly
NM_004369.4:c.8840C>G MANE Select	NP_004360.2:p.Ala2947Gly
NM_057166.5:c.7019C>G	NP_476507.3:p.Ala2340Gly
NM_057167.4:c.8222C>G	NP_476508.2:p.Ala2741Gly