Canonical Allele Identifier: CA1726782842
Gene: COL1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94426202C= , CM000669.2:g.94426202C= GRCh38
NC_000007.13:g.94055514C= , CM000669.1:g.94055514C= GRCh37
NC_000007.12:g.93893450C= NCBI36
NG_007405.1:g.36642C= , LRG_2:g.36642C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2997+151C= MANE Select ENSP00000297268.6:n.2997+151C=
ENST00000297268.10:c.2997+151C= ENSP00000297268.6:n.2997+151C=
ENST00000478215.1:n.556+151C=
ENST00000481570.5:n.2970+151C=
ENST00000620463.1:c.2991+151C= ENSP00000477719.1:n.2991+151C=
NM_000089.3:c.2997+151C= , LRG_2t1:c.2997+151C= NP_000080.2:n.2997+151C=
NM_000089.4:c.2997+151C= MANE Select NP_000080.2:n.2997+151C=
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