Canonical Allele Identifier: CA351218291

Gene: COL6A3

Linked Data

• ClinVar Variation Id: 1369803
• ClinVar RCV Id: RCV001894980
• dbSNP Id: rs2106370357
• MyVariant Identifiers: chr2:g.238290067G>A (hg19) ; chr2:g.237381424G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237381424G>A , CM000664.2:g.237381424G>A	GRCh38
NC_000002.11:g.238290067G>A , CM000664.1:g.238290067G>A	GRCh37
NC_000002.10:g.237954806G>A	NCBI36
NG_008676.1:g.37784C>T , LRG_473:g.37784C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000353578.9:c.770C>T	ENSP00000315873.4:p.Ala257Val
ENST00000682405.1:n.161C>T
ENST00000295550.9:c.1388C>T MANE Select	ENSP00000295550.4:p.Ala463Val
ENST00000295550.8:c.1388C>T	ENSP00000295550.4:p.Ala463Val
ENST00000347401.7:c.167C>T	ENSP00000315609.4:p.Ala56Val
ENST00000353578.8:c.770C>T	ENSP00000315873.4:p.Ala257Val
ENST00000392003.6:c.167C>T	ENSP00000375860.2:p.Ala56Val
ENST00000392004.7:c.770C>T	ENSP00000375861.3:p.Ala257Val
ENST00000409809.5:c.770C>T	ENSP00000386844.1:p.Ala257Val
ENST00000433762.1:c.1388C>T	ENSP00000389539.1:p.Ala463Val
ENST00000472056.5:c.167C>T	ENSP00000418285.1:p.Ala56Val
NM_004369.3:c.1388C>T , LRG_473t1:c.1388C>T	NP_004360.2:p.Ala463Val
NM_057164.4:c.167C>T	NP_476505.3:p.Ala56Val
NM_057165.4:c.770C>T	NP_476506.3:p.Ala257Val
NM_057166.4:c.167C>T	NP_476507.3:p.Ala56Val
NM_057167.3:c.770C>T	NP_476508.2:p.Ala257Val
XM_005246065.1:c.1388C>T	XP_005246122.1:p.Ala463Val
XM_005246066.1:c.167C>T	XP_005246123.1:p.Ala56Val
XM_006712253.1:c.1388C>T	XP_006712316.1:p.Ala463Val
XM_011510574.1:c.1388C>T	XP_011508876.1:p.Ala463Val
XM_011510575.1:c.92-4080C>T	XP_011508877.1:n.92-4080C>T
XM_017003304.1:c.92-4080C>T	XP_016858793.1:n.92-4080C>T
XM_024452684.1:c.167C>T	XP_024308452.1:p.Ala56Val
NM_004369.4:c.1388C>T MANE Select	NP_004360.2:p.Ala463Val
NM_057164.5:c.167C>T	NP_476505.3:p.Ala56Val
NM_057165.5:c.770C>T	NP_476506.3:p.Ala257Val
NM_057166.5:c.167C>T	NP_476507.3:p.Ala56Val
NM_057167.4:c.770C>T	NP_476508.2:p.Ala257Val