Canonical Allele Identifier: CA1726790991
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94401785G= , CM000669.2:g.94401785G= GRCh38
NC_000007.13:g.94031097G= , CM000669.1:g.94031097G= GRCh37
NC_000007.12:g.93869033G= NCBI36
NG_007405.1:g.12225G= , LRG_2:g.12225G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.279+165G= MANE Select ENSP00000297268.6:n.279+165G=
ENST00000297268.10:c.279+165G= ENSP00000297268.6:n.279+165G=
ENST00000620463.1:c.273+165G= ENSP00000477719.1:n.273+165G=
NM_000089.3:c.279+165G= , LRG_2t1:c.279+165G= NP_000080.2:n.279+165G=
NM_000089.4:c.279+165G= MANE Select NP_000080.2:n.279+165G=