Canonical Allele Identifier: CA1726792161
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404599C= , CM000669.2:g.94404599C= GRCh38
NC_000007.13:g.94033911C= , CM000669.1:g.94033911C= GRCh37
NC_000007.12:g.93871847C= NCBI36
NG_007405.1:g.15039C= , LRG_2:g.15039C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.323C= MANE Select ENSP00000297268.6:p.Pro108=
ENST00000297268.10:c.323C= ENSP00000297268.6:p.Pro108=
ENST00000620463.1:c.317C= ENSP00000477719.1:p.Pro106=
NM_000089.3:c.323C= , LRG_2t1:c.323C= NP_000080.2:p.Pro108=
NM_000089.4:c.323C= MANE Select NP_000080.2:p.Pro108=