Canonical Allele Identifier: CA766638857

Gene: COL6A3

Linked Data

• dbSNP Id: rs1288579663
• gnomAD v3: 2-237359307-A-G
• gnomAD v4: 2-237359307-A-G
• MyVariant Identifiers: chr2:g.238267950A>G (hg19) ; chr2:g.237359307A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237359307A>G , CM000664.2:g.237359307A>G	GRCh38
NC_000002.11:g.238267950A>G , CM000664.1:g.238267950A>G	GRCh37
NC_000002.10:g.237932689A>G	NCBI36
NG_008676.1:g.59901T>C , LRG_473:g.59901T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000353578.9:c.5691+55T>C	ENSP00000315873.4:n.5691+55T>C
ENST00000295550.9:c.6309+55T>C MANE Select	ENSP00000295550.4:n.6309+55T>C
ENST00000295550.8:c.6309+55T>C	ENSP00000295550.4:n.6309+55T>C
ENST00000347401.7:c.4488+55T>C	ENSP00000315609.4:n.4488+55T>C
ENST00000353578.8:c.5691+55T>C	ENSP00000315873.4:n.5691+55T>C
ENST00000409809.5:c.5691+55T>C	ENSP00000386844.1:n.5691+55T>C
ENST00000472056.5:c.4488+55T>C	ENSP00000418285.1:n.4488+55T>C
NM_004369.3:c.6309+55T>C , LRG_473t1:c.6309+55T>C	NP_004360.2:n.6309+55T>C
NM_057166.4:c.4488+55T>C	NP_476507.3:n.4488+55T>C
NM_057167.3:c.5691+55T>C	NP_476508.2:n.5691+55T>C
XM_005246065.1:c.5709+55T>C	XP_005246122.1:n.5709+55T>C
XM_005246066.1:c.5088+55T>C	XP_005246123.1:n.5088+55T>C
XM_006712253.1:c.5808+55T>C	XP_006712316.1:n.5808+55T>C
XM_011510574.1:c.6306+55T>C	XP_011508876.1:n.6306+55T>C
XM_011510575.1:c.3903+55T>C	XP_011508877.1:n.3903+55T>C
XM_017003304.1:c.3903+55T>C	XP_016858793.1:n.3903+55T>C
XM_024452684.1:c.5088+55T>C	XP_024308452.1:n.5088+55T>C
NM_004369.4:c.6309+55T>C MANE Select	NP_004360.2:n.6309+55T>C
NM_057166.5:c.4488+55T>C	NP_476507.3:n.4488+55T>C
NM_057167.4:c.5691+55T>C	NP_476508.2:n.5691+55T>C