Canonical Allele Identifier: CA62600080

Gene: COL5A2

Linked Data

• dbSNP Id: rs955935740
• gnomAD v3: 2-189058792-C-A
• gnomAD v4: 2-189058792-C-A
• MyVariant Identifiers: chr2:g.189923518C>A (hg19) ; chr2:g.189058792C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.189058792C>A , CM000664.2:g.189058792C>A	GRCh38
NC_000002.11:g.189923518C>A , CM000664.1:g.189923518C>A	GRCh37
NC_000002.10:g.189631763C>A	NCBI36
NG_011799.1:g.126088G>T
NG_011799.2:g.126088G>T
NG_011799.3:g.171510G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000374866.9:c.2130+57G>T MANE Select	ENSP00000364000.3:n.2130+57G>T
ENST00000374866.7:c.2130+57G>T	ENSP00000364000.3:n.2130+57G>T
ENST00000470524.2:n.236+57G>T
ENST00000618828.1:c.969+57G>T	ENSP00000482184.1:n.969+57G>T
NM_000393.3:c.2130+57G>T	NP_000384.2:n.2130+57G>T
XM_011510573.1:c.1992+57G>T	XP_011508875.1:n.1992+57G>T
NM_000393.4:c.2130+57G>T	NP_000384.2:n.2130+57G>T
XM_011510573.3:c.1992+57G>T	XP_011508875.1:n.1992+57G>T
NM_000393.5:c.2130+57G>T MANE Select	NP_000384.2:n.2130+57G>T