Canonical Allele Identifier: CA1726792148
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404580C= , CM000669.2:g.94404580C= GRCh38
NC_000007.13:g.94033892C= , CM000669.1:g.94033892C= GRCh37
NC_000007.12:g.93871828C= NCBI36
NG_007405.1:g.15020C= , LRG_2:g.15020C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.304C= MANE Select ENSP00000297268.6:p.Pro102=
ENST00000297268.10:c.304C= ENSP00000297268.6:p.Pro102=
ENST00000620463.1:c.298C= ENSP00000477719.1:p.Pro100=
NM_000089.3:c.304C= , LRG_2t1:c.304C= NP_000080.2:p.Pro102=
NM_000089.4:c.304C= MANE Select NP_000080.2:p.Pro102=