Canonical Allele Identifier: CA351202621

Gene: COL6A3

Linked Data

• gnomAD v4: 2-237344525-G-A
• MyVariant Identifiers: chr2:g.238253168G>A (hg19) ; chr2:g.237344525G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.237344525G>A , CM000664.2:g.237344525G>A	GRCh38
NC_000002.11:g.238253168G>A , CM000664.1:g.238253168G>A	GRCh37
NC_000002.10:g.237917907G>A	NCBI36
NG_008676.1:g.74683C>T , LRG_473:g.74683C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000347401.8:c.138C>T
ENST00000353578.9:c.6875C>T	ENSP00000315873.4:p.Thr2292Ile
ENST00000295550.9:c.7493C>T MANE Select	ENSP00000295550.4:p.Thr2498Ile
ENST00000295550.8:c.7493C>T	ENSP00000295550.4:p.Thr2498Ile
ENST00000347401.7:c.5669C>T	ENSP00000315609.4:p.Thr1890Ile
ENST00000353578.8:c.6875C>T	ENSP00000315873.4:p.Thr2292Ile
ENST00000409809.5:c.6875C>T	ENSP00000386844.1:p.Thr2292Ile
ENST00000472056.5:c.5672C>T	ENSP00000418285.1:p.Thr1891Ile
ENST00000491769.1:n.1747C>T
NM_004369.3:c.7493C>T , LRG_473t1:c.7493C>T	NP_004360.2:p.Thr2498Ile
NM_057166.4:c.5672C>T	NP_476507.3:p.Thr1891Ile
NM_057167.3:c.6875C>T	NP_476508.2:p.Thr2292Ile
XM_005246065.1:c.6893C>T	XP_005246122.1:p.Thr2298Ile
XM_005246066.1:c.6272C>T	XP_005246123.1:p.Thr2091Ile
XM_006712253.1:c.6992C>T	XP_006712316.1:p.Thr2331Ile
XM_011510574.1:c.7490C>T	XP_011508876.1:p.Thr2497Ile
XM_011510575.1:c.5087C>T	XP_011508877.1:p.Thr1696Ile
XM_017003304.1:c.5087C>T	XP_016858793.1:p.Thr1696Ile
XM_024452684.1:c.6272C>T	XP_024308452.1:p.Thr2091Ile
NM_004369.4:c.7493C>T MANE Select	NP_004360.2:p.Thr2498Ile
NM_057166.5:c.5672C>T	NP_476507.3:p.Thr1891Ile
NM_057167.4:c.6875C>T	NP_476508.2:p.Thr2292Ile