Canonical Allele Identifier: CA1726793775
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94408220G= , CM000669.2:g.94408220G= GRCh38
NC_000007.13:g.94037532G= , CM000669.1:g.94037532G= GRCh37
NC_000007.12:g.93875468G= NCBI36
NG_007405.1:g.18660G= , LRG_2:g.18660G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.677G= MANE Select ENSP00000297268.6:p.Gly226=
ENST00000297268.10:c.677G= ENSP00000297268.6:p.Gly226=
ENST00000620463.1:c.671G= ENSP00000477719.1:p.Gly224=
NM_000089.3:c.677G= , LRG_2t1:c.677G= NP_000080.2:p.Gly226=
NM_000089.4:c.677G= MANE Select NP_000080.2:p.Gly226=