Canonical Allele Identifier: CA349862899

Gene: COL5A2

Linked Data

• gnomAD v4: 2-189045903-T-C
• MyVariant Identifiers: chr2:g.189910629T>C (hg19) ; chr2:g.189045903T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189045903T>C , CM000664.2:g.189045903T>C	GRCh38
NC_000002.11:g.189910629T>C , CM000664.1:g.189910629T>C	GRCh37
NC_000002.10:g.189618874T>C	NCBI36
NG_011799.1:g.138977A>G
NG_011799.2:g.138977A>G
NG_011799.3:g.184399A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000374866.9:c.3206A>G MANE Select	ENSP00000364000.3:p.Asp1069Gly
ENST00000374866.7:c.3206A>G	ENSP00000364000.3:p.Asp1069Gly
ENST00000618828.1:c.2045A>G	ENSP00000482184.1:p.Asp682Gly
NM_000393.3:c.3206A>G	NP_000384.2:p.Asp1069Gly
XM_011510573.1:c.3068A>G	XP_011508875.1:p.Asp1023Gly
NM_000393.4:c.3206A>G	NP_000384.2:p.Asp1069Gly
XM_011510573.3:c.3068A>G	XP_011508875.1:p.Asp1023Gly
NM_000393.5:c.3206A>G MANE Select	NP_000384.2:p.Asp1069Gly