Canonical Allele Identifier: CA1726750796
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94409381A= , CM000669.2:g.94409381A= GRCh38
NC_000007.13:g.94038693A= , CM000669.1:g.94038693A= GRCh37
NC_000007.12:g.93876629A= NCBI36
NG_007405.1:g.19821A= , LRG_2:g.19821A=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.852A= MANE Select ENSP00000297268.6:p.Glu284=
ENST00000297268.10:c.852A= ENSP00000297268.6:p.Glu284=
ENST00000620463.1:c.846A= ENSP00000477719.1:p.Glu282=
NM_000089.3:c.852A= , LRG_2t1:c.852A= NP_000080.2:p.Glu284=
NM_000089.4:c.852A= MANE Select NP_000080.2:p.Glu284=