Canonical Allele Identifier: CA1726790999
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94401801T= , CM000669.2:g.94401801T= GRCh38
NC_000007.13:g.94031113T= , CM000669.1:g.94031113T= GRCh37
NC_000007.12:g.93869049T= NCBI36
NG_007405.1:g.12241T= , LRG_2:g.12241T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.279+181T= MANE Select ENSP00000297268.6:n.279+181T=
ENST00000297268.10:c.279+181T= ENSP00000297268.6:n.279+181T=
ENST00000620463.1:c.273+181T= ENSP00000477719.1:n.273+181T=
NM_000089.3:c.279+181T= , LRG_2t1:c.279+181T= NP_000080.2:n.279+181T=
NM_000089.4:c.279+181T= MANE Select NP_000080.2:n.279+181T=