Canonical Allele Identifier: CA62601071

Gene: COL5A2

Linked Data

• dbSNP Id: rs878959836
• MyVariant Identifiers: chr2:g.189927480T>A (hg19) ; chr2:g.189062754T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189062754T>A , CM000664.2:g.189062754T>A	GRCh38
NC_000002.11:g.189927480T>A , CM000664.1:g.189927480T>A	GRCh37
NC_000002.10:g.189635725T>A	NCBI36
NG_011799.1:g.122126A>T
NG_011799.2:g.122126A>T
NG_011799.3:g.167548A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374866.9:c.1977+111A>T MANE Select	ENSP00000364000.3:n.1977+111A>T
ENST00000374866.7:c.1977+111A>T	ENSP00000364000.3:n.1977+111A>T
ENST00000470524.2:n.83+111A>T
ENST00000618828.1:c.816+111A>T	ENSP00000482184.1:n.816+111A>T
NM_000393.3:c.1977+111A>T	NP_000384.2:n.1977+111A>T
XM_011510573.1:c.1839+111A>T	XP_011508875.1:n.1839+111A>T
NM_000393.4:c.1977+111A>T	NP_000384.2:n.1977+111A>T
XM_011510573.3:c.1839+111A>T	XP_011508875.1:n.1839+111A>T
NM_000393.5:c.1977+111A>T MANE Select	NP_000384.2:n.1977+111A>T