Canonical Allele Identifier: CA1726776857
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94423073T= , CM000669.2:g.94423073T= GRCh38
NC_000007.13:g.94052385T= , CM000669.1:g.94052385T= GRCh37
NC_000007.12:g.93890321T= NCBI36
NG_007405.1:g.33513T= , LRG_2:g.33513T=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2520T= MANE Select ENSP00000297268.6:p.Pro840=
ENST00000297268.10:c.2520T= ENSP00000297268.6:p.Pro840=
ENST00000481570.5:n.603T=
ENST00000497316.5:n.917T=
ENST00000620463.1:c.2514T= ENSP00000477719.1:p.Pro838=
NM_000089.3:c.2520T= , LRG_2t1:c.2520T= NP_000080.2:p.Pro840=
NM_000089.4:c.2520T= MANE Select NP_000080.2:p.Pro840=