Canonical Allele Identifier: CA1726792147
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404576C= , CM000669.2:g.94404576C= GRCh38
NC_000007.13:g.94033888C= , CM000669.1:g.94033888C= GRCh37
NC_000007.12:g.93871824C= NCBI36
NG_007405.1:g.15016C= , LRG_2:g.15016C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.300C= MANE Select ENSP00000297268.6:p.Gly100=
ENST00000297268.10:c.300C= ENSP00000297268.6:p.Gly100=
ENST00000620463.1:c.294C= ENSP00000477719.1:p.Gly98=
NM_000089.3:c.300C= , LRG_2t1:c.300C= NP_000080.2:p.Gly100=
NM_000089.4:c.300C= MANE Select NP_000080.2:p.Gly100=