Canonical Allele Identifier: CA1726790995
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94401797T= , CM000669.2:g.94401797T= GRCh38
NC_000007.13:g.94031109T= , CM000669.1:g.94031109T= GRCh37
NC_000007.12:g.93869045T= NCBI36
NG_007405.1:g.12237T= , LRG_2:g.12237T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.279+177T= MANE Select ENSP00000297268.6:n.279+177T=
ENST00000297268.10:c.279+177T= ENSP00000297268.6:n.279+177T=
ENST00000620463.1:c.273+177T= ENSP00000477719.1:n.273+177T=
NM_000089.3:c.279+177T= , LRG_2t1:c.279+177T= NP_000080.2:n.279+177T=
NM_000089.4:c.279+177T= MANE Select NP_000080.2:n.279+177T=