Canonical Allele Identifier: CA1726778564
Gene: COL1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94424288A= , CM000669.2:g.94424288A= GRCh38
NC_000007.13:g.94053600A= , CM000669.1:g.94053600A= GRCh37
NC_000007.12:g.93891536A= NCBI36
NG_007405.1:g.34728A= , LRG_2:g.34728A=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2566-48A= MANE Select ENSP00000297268.6:n.2566-48A=
ENST00000297268.10:c.2566-48A= ENSP00000297268.6:n.2566-48A=
ENST00000469732.1:n.301A=
ENST00000481570.5:n.1818A=
ENST00000620463.1:c.2560-48A= ENSP00000477719.1:n.2560-48A=
NM_000089.3:c.2566-48A= , LRG_2t1:c.2566-48A= NP_000080.2:n.2566-48A=
NM_000089.4:c.2566-48A= MANE Select NP_000080.2:n.2566-48A=
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