Canonical Allele Identifier: CA339874690

Gene: COL9A2

Linked Data

• MyVariant Identifiers: chr1:g.40767520C>G (hg19) ; chr1:g.40301848C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.40301848C>G , CM000663.2:g.40301848C>G	GRCh38
NC_000001.10:g.40767520C>G , CM000663.1:g.40767520C>G	GRCh37
NC_000001.9:g.40540107C>G	NCBI36
NG_008031.1:g.20420G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372748.8:c.1834G>C MANE Select	ENSP00000361834.3:p.Gly612Arg
ENST00000372748.7:c.1834G>C	ENSP00000361834.3:p.Gly612Arg
ENST00000466267.1:n.799G>C
ENST00000482722.5:n.2137G>C
NM_001852.3:c.1834G>C	NP_001843.1:p.Gly612Arg
XM_006710365.2:c.1834G>C	XP_006710428.1:p.Gly612Arg
XM_011540714.1:c.1846G>C	XP_011539016.1:p.Gly616Arg
XM_011540715.1:c.1564G>C	XP_011539017.1:p.Gly522Arg
XM_011540716.1:c.1564G>C	XP_011539018.1:p.Gly522Arg
XM_011540717.1:c.1291G>C	XP_011539019.1:p.Gly431Arg
XM_006710365.3:c.1834G>C	XP_006710428.1:p.Gly612Arg
XM_011540715.2:c.1564G>C	XP_011539017.1:p.Gly522Arg
XM_011540716.2:c.1564G>C	XP_011539018.1:p.Gly522Arg
XM_011540717.2:c.1291G>C	XP_011539019.1:p.Gly431Arg
XM_017000332.1:c.1846G>C	XP_016855821.1:p.Gly616Arg
XM_017000333.1:c.1552G>C	XP_016855822.1:p.Gly518Arg
NM_001852.4:c.1834G>C MANE Select	NP_001843.1:p.Gly612Arg