Canonical Allele Identifier: CA540463671

Gene: COL6A3

Linked Data

• dbSNP Id: rs1348604114
• gnomAD v2: 2-238267841-T-A
• gnomAD v4: 2-237359198-T-A
• MyVariant Identifiers: chr2:g.238267841T>A (hg19) ; chr2:g.237359198T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237359198T>A , CM000664.2:g.237359198T>A	GRCh38
NC_000002.11:g.238267841T>A , CM000664.1:g.238267841T>A	GRCh37
NC_000002.10:g.237932580T>A	NCBI36
NG_008676.1:g.60010A>T , LRG_473:g.60010A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000353578.9:c.5736+8A>T	ENSP00000315873.4:n.5736+8A>T
ENST00000295550.9:c.6354+8A>T MANE Select	ENSP00000295550.4:n.6354+8A>T
ENST00000295550.8:c.6354+8A>T	ENSP00000295550.4:n.6354+8A>T
ENST00000347401.7:c.4533+8A>T	ENSP00000315609.4:n.4533+8A>T
ENST00000353578.8:c.5736+8A>T	ENSP00000315873.4:n.5736+8A>T
ENST00000409809.5:c.5736+8A>T	ENSP00000386844.1:n.5736+8A>T
ENST00000472056.5:c.4533+8A>T	ENSP00000418285.1:n.4533+8A>T
NM_004369.3:c.6354+8A>T , LRG_473t1:c.6354+8A>T	NP_004360.2:n.6354+8A>T
NM_057166.4:c.4533+8A>T	NP_476507.3:n.4533+8A>T
NM_057167.3:c.5736+8A>T	NP_476508.2:n.5736+8A>T
XM_005246065.1:c.5754+8A>T	XP_005246122.1:n.5754+8A>T
XM_005246066.1:c.5133+8A>T	XP_005246123.1:n.5133+8A>T
XM_006712253.1:c.5853+8A>T	XP_006712316.1:n.5853+8A>T
XM_011510574.1:c.6351+8A>T	XP_011508876.1:n.6351+8A>T
XM_011510575.1:c.3948+8A>T	XP_011508877.1:n.3948+8A>T
XM_017003304.1:c.3948+8A>T	XP_016858793.1:n.3948+8A>T
XM_024452684.1:c.5133+8A>T	XP_024308452.1:n.5133+8A>T
NM_004369.4:c.6354+8A>T MANE Select	NP_004360.2:n.6354+8A>T
NM_057166.5:c.4533+8A>T	NP_476507.3:n.4533+8A>T
NM_057167.4:c.5736+8A>T	NP_476508.2:n.5736+8A>T