Canonical Allele Identifier: CA1726777001
Gene: COL1A2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94423112T= , CM000669.2:g.94423112T= GRCh38
NC_000007.13:g.94052424T= , CM000669.1:g.94052424T= GRCh37
NC_000007.12:g.93890360T= NCBI36
NG_007405.1:g.33552T= , LRG_2:g.33552T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2559T= MANE Select ENSP00000297268.6:p.Gly853=
ENST00000297268.10:c.2559T= ENSP00000297268.6:p.Gly853=
ENST00000481570.5:n.642T=
ENST00000497316.5:n.956T=
ENST00000620463.1:c.2553T= ENSP00000477719.1:p.Gly851=
NM_000089.3:c.2559T= , LRG_2t1:c.2559T= NP_000080.2:p.Gly853=
NM_000089.4:c.2559T= MANE Select NP_000080.2:p.Gly853=
Search 100 bp 5'
Search 100 bp 3'