Canonical Allele Identifier: CA1726777242
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94423240G= , CM000669.2:g.94423240G= GRCh38
NC_000007.13:g.94052552G= , CM000669.1:g.94052552G= GRCh37
NC_000007.12:g.93890488G= NCBI36
NG_007405.1:g.33680G= , LRG_2:g.33680G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2565+122G= MANE Select ENSP00000297268.6:n.2565+122G=
ENST00000297268.10:c.2565+122G= ENSP00000297268.6:n.2565+122G=
ENST00000481570.5:n.770G=
ENST00000620463.1:c.2559+122G= ENSP00000477719.1:n.2559+122G=
NM_000089.3:c.2565+122G= , LRG_2t1:c.2565+122G= NP_000080.2:n.2565+122G=
NM_000089.4:c.2565+122G= MANE Select NP_000080.2:n.2565+122G=