Canonical Allele Identifier: CA1726776836
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94423068C= , CM000669.2:g.94423068C= GRCh38
NC_000007.13:g.94052380C= , CM000669.1:g.94052380C= GRCh37
NC_000007.12:g.93890316C= NCBI36
NG_007405.1:g.33508C= , LRG_2:g.33508C=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2515C= MANE Select ENSP00000297268.6:p.Pro839=
ENST00000297268.10:c.2515C= ENSP00000297268.6:p.Pro839=
ENST00000481570.5:n.598C=
ENST00000497316.5:n.912C=
ENST00000620463.1:c.2509C= ENSP00000477719.1:p.Pro837=
NM_000089.3:c.2515C= , LRG_2t1:c.2515C= NP_000080.2:p.Pro839=
NM_000089.4:c.2515C= MANE Select NP_000080.2:p.Pro839=