Canonical Allele Identifier: CA351195098

Gene: COL6A3

Linked Data

• dbSNP Id: rs1574939389
• MyVariant Identifiers: chr2:g.238249211A>C (hg19) ; chr2:g.237340568A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237340568A>C , CM000664.2:g.237340568A>C	GRCh38
NC_000002.11:g.238249211A>C , CM000664.1:g.238249211A>C	GRCh37
NC_000002.10:g.237913950A>C	NCBI36
NG_008676.1:g.78640T>G , LRG_473:g.78640T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.993T>G
ENST00000353578.9:c.7730T>G	ENSP00000315873.4:p.Val2577Gly
ENST00000682957.1:c.351T>G
ENST00000684508.1:n.615T>G
ENST00000295550.9:c.8348T>G MANE Select	ENSP00000295550.4:p.Val2783Gly
ENST00000295550.8:c.8348T>G	ENSP00000295550.4:p.Val2783Gly
ENST00000347401.7:c.6524T>G	ENSP00000315609.4:p.Val2175Gly
ENST00000353578.8:c.7730T>G	ENSP00000315873.4:p.Val2577Gly
ENST00000409809.5:c.7730T>G	ENSP00000386844.1:p.Val2577Gly
ENST00000468792.1:n.35T>G
ENST00000472056.5:c.6527T>G	ENSP00000418285.1:p.Val2176Gly
ENST00000491769.1:n.4790T>G
NM_004369.3:c.8348T>G , LRG_473t1:c.8348T>G	NP_004360.2:p.Val2783Gly
NM_057166.4:c.6527T>G	NP_476507.3:p.Val2176Gly
NM_057167.3:c.7730T>G	NP_476508.2:p.Val2577Gly
XM_005246065.1:c.7748T>G	XP_005246122.1:p.Val2583Gly
XM_005246066.1:c.7127T>G	XP_005246123.1:p.Val2376Gly
XM_006712253.1:c.7847T>G	XP_006712316.1:p.Val2616Gly
XM_011510574.1:c.8345T>G	XP_011508876.1:p.Val2782Gly
XM_011510575.1:c.5942T>G	XP_011508877.1:p.Val1981Gly
XM_017003304.1:c.5942T>G	XP_016858793.1:p.Val1981Gly
XM_024452684.1:c.7127T>G	XP_024308452.1:p.Val2376Gly
NM_004369.4:c.8348T>G MANE Select	NP_004360.2:p.Val2783Gly
NM_057166.5:c.6527T>G	NP_476507.3:p.Val2176Gly
NM_057167.4:c.7730T>G	NP_476508.2:p.Val2577Gly