Canonical Allele Identifier: CA2187777

Gene: COL6A3

Linked Data

• dbSNP Id: rs757907869
• ExAC: 2:238253096 G / A
• gnomAD v2: 2-238253096-G-A
• gnomAD v4: 2-237344453-G-A
• MyVariant Identifiers: chr2:g.238253096G>A (hg19) ; chr2:g.237344453G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344453G>A , CM000664.2:g.237344453G>A	GRCh38
NC_000002.11:g.238253096G>A , CM000664.1:g.238253096G>A	GRCh37
NC_000002.10:g.237917835G>A	NCBI36
NG_008676.1:g.74755C>T , LRG_473:g.74755C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.210C>T
ENST00000353578.9:c.6947C>T	ENSP00000315873.4:p.Ala2316Val
ENST00000295550.9:c.7565C>T MANE Select	ENSP00000295550.4:p.Ala2522Val
ENST00000295550.8:c.7565C>T	ENSP00000295550.4:p.Ala2522Val
ENST00000347401.7:c.5741C>T	ENSP00000315609.4:p.Ala1914Val
ENST00000353578.8:c.6947C>T	ENSP00000315873.4:p.Ala2316Val
ENST00000409809.5:c.6947C>T	ENSP00000386844.1:p.Ala2316Val
ENST00000472056.5:c.5744C>T	ENSP00000418285.1:p.Ala1915Val
ENST00000491769.1:n.1819C>T
NM_004369.3:c.7565C>T , LRG_473t1:c.7565C>T	NP_004360.2:p.Ala2522Val
NM_057166.4:c.5744C>T	NP_476507.3:p.Ala1915Val
NM_057167.3:c.6947C>T	NP_476508.2:p.Ala2316Val
XM_005246065.1:c.6965C>T	XP_005246122.1:p.Ala2322Val
XM_005246066.1:c.6344C>T	XP_005246123.1:p.Ala2115Val
XM_006712253.1:c.7064C>T	XP_006712316.1:p.Ala2355Val
XM_011510574.1:c.7562C>T	XP_011508876.1:p.Ala2521Val
XM_011510575.1:c.5159C>T	XP_011508877.1:p.Ala1720Val
XM_017003304.1:c.5159C>T	XP_016858793.1:p.Ala1720Val
XM_024452684.1:c.6344C>T	XP_024308452.1:p.Ala2115Val
NM_004369.4:c.7565C>T MANE Select	NP_004360.2:p.Ala2522Val
NM_057166.5:c.5744C>T	NP_476507.3:p.Ala1915Val
NM_057167.4:c.6947C>T	NP_476508.2:p.Ala2316Val