Canonical Allele Identifier: CA1726783160
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94426441G= , CM000669.2:g.94426441G= GRCh38
NC_000007.13:g.94055753G= , CM000669.1:g.94055753G= GRCh37
NC_000007.12:g.93893689G= NCBI36
NG_007405.1:g.36881G= , LRG_2:g.36881G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.3016G= MANE Select ENSP00000297268.6:p.Gly1006=
ENST00000297268.10:c.3016G= ENSP00000297268.6:p.Gly1006=
ENST00000478215.1:n.575G=
ENST00000481570.5:n.2989G=
ENST00000620463.1:c.3010G= ENSP00000477719.1:p.Gly1004=
NM_000089.3:c.3016G= , LRG_2t1:c.3016G= NP_000080.2:p.Gly1006=
NM_000089.4:c.3016G= MANE Select NP_000080.2:p.Gly1006=