Canonical Allele Identifier: CA430324393
Gene: COL5A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189927606A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189062880A>G , CM000664.2:g.189062880A>G GRCh38
NC_000002.11:g.189927606A>G , CM000664.1:g.189927606A>G GRCh37
NC_000002.10:g.189635851A>G NCBI36
NG_011799.1:g.122000T>C
NG_011799.2:g.122000T>C
NG_011799.3:g.167422T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000374866.9:c.1962T>C MANE Select ENSP00000364000.3:p.Gly654=
ENST00000374866.7:c.1962T>C ENSP00000364000.3:p.Gly654=
ENST00000470524.2:n.68T>C
ENST00000618828.1:c.801T>C ENSP00000482184.1:p.Gly267=
NM_000393.3:c.1962T>C NP_000384.2:p.Gly654=
XM_011510573.1:c.1824T>C XP_011508875.1:p.Gly608=
NM_000393.4:c.1962T>C NP_000384.2:p.Gly654=
XM_011510573.3:c.1824T>C XP_011508875.1:p.Gly608=
NM_000393.5:c.1962T>C MANE Select NP_000384.2:p.Gly654=