Canonical Allele Identifier: CA2188984

Gene: COL6A3

Linked Data

• ClinVar Variation Id: 593964
• ClinVar RCV Id: RCV000729151 ; RCV001411344
• dbSNP Id: rs761804539
• ExAC: 2:238280505 G / A
• gnomAD v2: 2-238280505-G-A
• gnomAD v3: 2-237371862-G-A
• gnomAD v4: 2-237371862-G-A
• COSMIC: COSM4092649 ; COSM4092650
• MyVariant Identifiers: chr2:g.238280505G>A (hg19) ; chr2:g.237371862G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237371862G>A , CM000664.2:g.237371862G>A	GRCh38
NC_000002.11:g.238280505G>A , CM000664.1:g.238280505G>A	GRCh37
NC_000002.10:g.237945244G>A	NCBI36
NG_008676.1:g.47346C>T , LRG_473:g.47346C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353578.9:c.3537C>T	ENSP00000315873.4:p.Pro1179=
ENST00000295550.9:c.4155C>T MANE Select	ENSP00000295550.4:p.Pro1385=
ENST00000295550.8:c.4155C>T	ENSP00000295550.4:p.Pro1385=
ENST00000347401.7:c.2334C>T	ENSP00000315609.4:p.Pro778=
ENST00000353578.8:c.3537C>T	ENSP00000315873.4:p.Pro1179=
ENST00000392003.6:c.2934C>T	ENSP00000375860.2:p.Pro978=
ENST00000392004.7:c.3537C>T	ENSP00000375861.3:p.Pro1179=
ENST00000409809.5:c.3537C>T	ENSP00000386844.1:p.Pro1179=
ENST00000472056.5:c.2334C>T	ENSP00000418285.1:p.Pro778=
NM_004369.3:c.4155C>T , LRG_473t1:c.4155C>T	NP_004360.2:p.Pro1385=
NM_057164.4:c.2934C>T	NP_476505.3:p.Pro978=
NM_057165.4:c.3537C>T	NP_476506.3:p.Pro1179=
NM_057166.4:c.2334C>T	NP_476507.3:p.Pro778=
NM_057167.3:c.3537C>T	NP_476508.2:p.Pro1179=
XM_005246065.1:c.3555C>T	XP_005246122.1:p.Pro1185=
XM_005246066.1:c.2934C>T	XP_005246123.1:p.Pro978=
XM_006712253.1:c.4155C>T	XP_006712316.1:p.Pro1385=
XM_011510574.1:c.4155C>T	XP_011508876.1:p.Pro1385=
XM_011510575.1:c.1749C>T	XP_011508877.1:p.Pro583=
XM_017003304.1:c.1749C>T	XP_016858793.1:p.Pro583=
XM_024452684.1:c.2934C>T	XP_024308452.1:p.Pro978=
NM_004369.4:c.4155C>T MANE Select	NP_004360.2:p.Pro1385=
NM_057164.5:c.2934C>T	NP_476505.3:p.Pro978=
NM_057165.5:c.3537C>T	NP_476506.3:p.Pro1179=
NM_057166.5:c.2334C>T	NP_476507.3:p.Pro778=
NM_057167.4:c.3537C>T	NP_476508.2:p.Pro1179=