Canonical Allele Identifier: CA1726779046
Gene: COL1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94424444G= , CM000669.2:g.94424444G= GRCh38
NC_000007.13:g.94053756G= , CM000669.1:g.94053756G= GRCh37
NC_000007.12:g.93891692G= NCBI36
NG_007405.1:g.34884G= , LRG_2:g.34884G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2673+1G= MANE Select ENSP00000297268.6:n.2673+1G=
ENST00000297268.10:c.2673+1G= ENSP00000297268.6:n.2673+1G=
ENST00000469732.1:n.456+1G=
ENST00000481570.5:n.1974G=
ENST00000620463.1:c.2667+1G= ENSP00000477719.1:n.2667+1G=
NM_000089.3:c.2673+1G= , LRG_2t1:c.2673+1G= NP_000080.2:n.2673+1G=
NM_000089.4:c.2673+1G= MANE Select NP_000080.2:n.2673+1G=
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