Canonical Allele Identifier: CA1726748334
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94408224C= , CM000669.2:g.94408224C= GRCh38
NC_000007.13:g.94037536C= , CM000669.1:g.94037536C= GRCh37
NC_000007.12:g.93875472C= NCBI36
NG_007405.1:g.18664C= , LRG_2:g.18664C=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.681C= MANE Select ENSP00000297268.6:p.Ala227=
ENST00000297268.10:c.681C= ENSP00000297268.6:p.Ala227=
ENST00000620463.1:c.675C= ENSP00000477719.1:p.Ala225=
NM_000089.3:c.681C= , LRG_2t1:c.681C= NP_000080.2:p.Ala227=
NM_000089.4:c.681C= MANE Select NP_000080.2:p.Ala227=