Canonical Allele Identifier: CA1726793777
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94408222G= , CM000669.2:g.94408222G= GRCh38
NC_000007.13:g.94037534G= , CM000669.1:g.94037534G= GRCh37
NC_000007.12:g.93875470G= NCBI36
NG_007405.1:g.18662G= , LRG_2:g.18662G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.679G= MANE Select ENSP00000297268.6:p.Ala227=
ENST00000297268.10:c.679G= ENSP00000297268.6:p.Ala227=
ENST00000620463.1:c.673G= ENSP00000477719.1:p.Ala225=
NM_000089.3:c.679G= , LRG_2t1:c.679G= NP_000080.2:p.Ala227=
NM_000089.4:c.679G= MANE Select NP_000080.2:p.Ala227=