Canonical Allele Identifier: CA1726767640
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94417796G= , CM000669.2:g.94417796G= GRCh38
NC_000007.13:g.94047108G= , CM000669.1:g.94047108G= GRCh37
NC_000007.12:g.93885044G= NCBI36
NG_007405.1:g.28236G= , LRG_2:g.28236G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.1936G= MANE Select ENSP00000297268.6:p.Gly646=
ENST00000297268.10:c.1936G= ENSP00000297268.6:p.Gly646=
ENST00000461525.5:n.25G=
ENST00000473573.5:n.273G=
ENST00000497316.5:n.333G=
ENST00000620463.1:c.1930G= ENSP00000477719.1:p.Gly644=
NM_000089.3:c.1936G= , LRG_2t1:c.1936G= NP_000080.2:p.Gly646=
NM_000089.4:c.1936G= MANE Select NP_000080.2:p.Gly646=