Canonical Allele Identifier: CA1726748342
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94408225C= , CM000669.2:g.94408225C= GRCh38
NC_000007.13:g.94037537C= , CM000669.1:g.94037537C= GRCh37
NC_000007.12:g.93875473C= NCBI36
NG_007405.1:g.18665C= , LRG_2:g.18665C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.682C= MANE Select ENSP00000297268.6:p.Pro228=
ENST00000297268.10:c.682C= ENSP00000297268.6:p.Pro228=
ENST00000620463.1:c.676C= ENSP00000477719.1:p.Pro226=
NM_000089.3:c.682C= , LRG_2t1:c.682C= NP_000080.2:p.Pro228=
NM_000089.4:c.682C= MANE Select NP_000080.2:p.Pro228=