Canonical Allele Identifier: CA1726778572
Gene: COL1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94424296G= , CM000669.2:g.94424296G= GRCh38
NC_000007.13:g.94053608G= , CM000669.1:g.94053608G= GRCh37
NC_000007.12:g.93891544G= NCBI36
NG_007405.1:g.34736G= , LRG_2:g.34736G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2566-40G= MANE Select ENSP00000297268.6:n.2566-40G=
ENST00000297268.10:c.2566-40G= ENSP00000297268.6:n.2566-40G=
ENST00000469732.1:n.309G=
ENST00000481570.5:n.1826G=
ENST00000620463.1:c.2560-40G= ENSP00000477719.1:n.2560-40G=
NM_000089.3:c.2566-40G= , LRG_2t1:c.2566-40G= NP_000080.2:n.2566-40G=
NM_000089.4:c.2566-40G= MANE Select NP_000080.2:n.2566-40G=
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