Canonical Allele Identifier: CA67830758

Gene: COL6A3

Linked Data

• dbSNP Id: rs1033933584
• MyVariant Identifiers: chr2:g.238245131A>G (hg19) ; chr2:g.237336488A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336488A>G , CM000664.2:g.237336488A>G	GRCh38
NC_000002.11:g.238245131A>G , CM000664.1:g.238245131A>G	GRCh37
NC_000002.10:g.237909870A>G	NCBI36
NG_008676.1:g.82720T>C , LRG_473:g.82720T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1257T>C
ENST00000353578.9:c.7994T>C	ENSP00000315873.4:p.Val2665Ala
ENST00000682957.1:c.739T>C
ENST00000684508.1:n.879T>C
ENST00000295550.9:c.8612T>C MANE Select	ENSP00000295550.4:p.Val2871Ala
ENST00000295550.8:c.8612T>C	ENSP00000295550.4:p.Val2871Ala
ENST00000347401.7:c.6788T>C	ENSP00000315609.4:p.Val2263Ala
ENST00000353578.8:c.7994T>C	ENSP00000315873.4:p.Val2665Ala
ENST00000409809.5:c.7994T>C	ENSP00000386844.1:p.Val2665Ala
ENST00000472056.5:c.6791T>C	ENSP00000418285.1:p.Val2264Ala
ENST00000491769.1:n.5054T>C
NM_004369.3:c.8612T>C , LRG_473t1:c.8612T>C	NP_004360.2:p.Val2871Ala
NM_057166.4:c.6791T>C	NP_476507.3:p.Val2264Ala
NM_057167.3:c.7994T>C	NP_476508.2:p.Val2665Ala
XM_005246065.1:c.8012T>C	XP_005246122.1:p.Val2671Ala
XM_005246066.1:c.7391T>C	XP_005246123.1:p.Val2464Ala
XM_006712253.1:c.8111T>C	XP_006712316.1:p.Val2704Ala
XM_011510574.1:c.8609T>C	XP_011508876.1:p.Val2870Ala
XM_011510575.1:c.6206T>C	XP_011508877.1:p.Val2069Ala
XM_017003304.1:c.6206T>C	XP_016858793.1:p.Val2069Ala
XM_024452684.1:c.7391T>C	XP_024308452.1:p.Val2464Ala
NM_004369.4:c.8612T>C MANE Select	NP_004360.2:p.Val2871Ala
NM_057166.5:c.6791T>C	NP_476507.3:p.Val2264Ala
NM_057167.4:c.7994T>C	NP_476508.2:p.Val2665Ala