Canonical Allele Identifier: CA1726749281
Gene: COL1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94408721C= , CM000669.2:g.94408721C= GRCh38
NC_000007.13:g.94038033C= , CM000669.1:g.94038033C= GRCh37
NC_000007.12:g.93875969C= NCBI36
NG_007405.1:g.19161C= , LRG_2:g.19161C=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.739-49C= MANE Select ENSP00000297268.6:n.739-49C=
ENST00000297268.10:c.739-49C= ENSP00000297268.6:n.739-49C=
ENST00000620463.1:c.733-49C= ENSP00000477719.1:n.733-49C=
NM_000089.3:c.739-49C= , LRG_2t1:c.739-49C= NP_000080.2:n.739-49C=
NM_000089.4:c.739-49C= MANE Select NP_000080.2:n.739-49C=
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