Canonical Allele Identifier: CA1726782435
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94426014T= , CM000669.2:g.94426014T= GRCh38
NC_000007.13:g.94055326T= , CM000669.1:g.94055326T= GRCh37
NC_000007.12:g.93893262T= NCBI36
NG_007405.1:g.36454T= , LRG_2:g.36454T=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2960T= MANE Select ENSP00000297268.6:p.Val987=
ENST00000297268.10:c.2960T= ENSP00000297268.6:p.Val987=
ENST00000478215.1:n.519T=
ENST00000481570.5:n.2933T=
ENST00000620463.1:c.2954T= ENSP00000477719.1:p.Val985=
NM_000089.3:c.2960T= , LRG_2t1:c.2960T= NP_000080.2:p.Val987=
NM_000089.4:c.2960T= MANE Select NP_000080.2:p.Val987=