Canonical Allele Identifier: CA1726767736
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94417803C= , CM000669.2:g.94417803C= GRCh38
NC_000007.13:g.94047115C= , CM000669.1:g.94047115C= GRCh37
NC_000007.12:g.93885051C= NCBI36
NG_007405.1:g.28243C= , LRG_2:g.28243C=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.1943C= MANE Select ENSP00000297268.6:p.Ala648=
ENST00000297268.10:c.1943C= ENSP00000297268.6:p.Ala648=
ENST00000461525.5:n.32C=
ENST00000473573.5:n.280C=
ENST00000497316.5:n.340C=
ENST00000620463.1:c.1937C= ENSP00000477719.1:p.Ala646=
NM_000089.3:c.1943C= , LRG_2t1:c.1943C= NP_000080.2:p.Ala648=
NM_000089.4:c.1943C= MANE Select NP_000080.2:p.Ala648=