Canonical Allele Identifier: CA431702009

Gene: COL6A3

Linked Data

• dbSNP Id: rs1332418093
• gnomAD v2: 2-238244989-C-A
• gnomAD v3: 2-237336346-C-A
• gnomAD v4: 2-237336346-C-A
• MyVariant Identifiers: chr2:g.238244989C>A (hg19) ; chr2:g.237336346C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237336346C>A , CM000664.2:g.237336346C>A	GRCh38
NC_000002.11:g.238244989C>A , CM000664.1:g.238244989C>A	GRCh37
NC_000002.10:g.237909728C>A	NCBI36
NG_008676.1:g.82862G>T , LRG_473:g.82862G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.1399G>T
ENST00000353578.9:c.8136G>T	ENSP00000315873.4:p.Val2712=
ENST00000682957.1:c.881G>T
ENST00000684508.1:n.1021G>T
ENST00000295550.9:c.8754G>T MANE Select	ENSP00000295550.4:p.Val2918=
ENST00000295550.8:c.8754G>T	ENSP00000295550.4:p.Val2918=
ENST00000347401.7:c.6930G>T	ENSP00000315609.4:p.Val2310=
ENST00000353578.8:c.8136G>T	ENSP00000315873.4:p.Val2712=
ENST00000409809.5:c.8136G>T	ENSP00000386844.1:p.Val2712=
ENST00000472056.5:c.6933G>T	ENSP00000418285.1:p.Val2311=
ENST00000491769.1:n.5196G>T
NM_004369.3:c.8754G>T , LRG_473t1:c.8754G>T	NP_004360.2:p.Val2918=
NM_057166.4:c.6933G>T	NP_476507.3:p.Val2311=
NM_057167.3:c.8136G>T	NP_476508.2:p.Val2712=
XM_005246065.1:c.8154G>T	XP_005246122.1:p.Val2718=
XM_005246066.1:c.7533G>T	XP_005246123.1:p.Val2511=
XM_006712253.1:c.8253G>T	XP_006712316.1:p.Val2751=
XM_011510574.1:c.8751G>T	XP_011508876.1:p.Val2917=
XM_011510575.1:c.6348G>T	XP_011508877.1:p.Val2116=
XM_017003304.1:c.6348G>T	XP_016858793.1:p.Val2116=
XM_024452684.1:c.7533G>T	XP_024308452.1:p.Val2511=
NM_004369.4:c.8754G>T MANE Select	NP_004360.2:p.Val2918=
NM_057166.5:c.6933G>T	NP_476507.3:p.Val2311=
NM_057167.4:c.8136G>T	NP_476508.2:p.Val2712=