Canonical Allele Identifier: CA1726792128
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404541C= , CM000669.2:g.94404541C= GRCh38
NC_000007.13:g.94033853C= , CM000669.1:g.94033853C= GRCh37
NC_000007.12:g.93871789C= NCBI36
NG_007405.1:g.14981C= , LRG_2:g.14981C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.280-15C= MANE Select ENSP00000297268.6:n.280-15C=
ENST00000297268.10:c.280-15C= ENSP00000297268.6:n.280-15C=
ENST00000620463.1:c.274-15C= ENSP00000477719.1:n.274-15C=
NM_000089.3:c.280-15C= , LRG_2t1:c.280-15C= NP_000080.2:n.280-15C=
NM_000089.4:c.280-15C= MANE Select NP_000080.2:n.280-15C=