Canonical Allele Identifier: CA1726776964
Gene: COL1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94423095C= , CM000669.2:g.94423095C= GRCh38
NC_000007.13:g.94052407C= , CM000669.1:g.94052407C= GRCh37
NC_000007.12:g.93890343C= NCBI36
NG_007405.1:g.33535C= , LRG_2:g.33535C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2542C= MANE Select ENSP00000297268.6:p.Pro848=
ENST00000297268.10:c.2542C= ENSP00000297268.6:p.Pro848=
ENST00000481570.5:n.625C=
ENST00000497316.5:n.939C=
ENST00000620463.1:c.2536C= ENSP00000477719.1:p.Pro846=
NM_000089.3:c.2542C= , LRG_2t1:c.2542C= NP_000080.2:p.Pro848=
NM_000089.4:c.2542C= MANE Select NP_000080.2:p.Pro848=
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