Canonical Allele Identifier: CA1726792113
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404513A= , CM000669.2:g.94404513A= GRCh38
NC_000007.13:g.94033825A= , CM000669.1:g.94033825A= GRCh37
NC_000007.12:g.93871761A= NCBI36
NG_007405.1:g.14953A= , LRG_2:g.14953A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.280-43A= MANE Select ENSP00000297268.6:n.280-43A=
ENST00000297268.10:c.280-43A= ENSP00000297268.6:n.280-43A=
ENST00000620463.1:c.274-43A= ENSP00000477719.1:n.274-43A=
NM_000089.3:c.280-43A= , LRG_2t1:c.280-43A= NP_000080.2:n.280-43A=
NM_000089.4:c.280-43A= MANE Select NP_000080.2:n.280-43A=