Canonical Allele Identifier: CA1726792228
Gene: COL1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404772A= , CM000669.2:g.94404772A= GRCh38
NC_000007.13:g.94034084A= , CM000669.1:g.94034084A= GRCh37
NC_000007.12:g.93872020A= NCBI36
NG_007405.1:g.15212A= , LRG_2:g.15212A=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.378+26A= MANE Select ENSP00000297268.6:n.378+26A=
ENST00000297268.10:c.378+26A= ENSP00000297268.6:n.378+26A=
ENST00000620463.1:c.372+26A= ENSP00000477719.1:n.372+26A=
NM_000089.3:c.378+26A= , LRG_2t1:c.378+26A= NP_000080.2:n.378+26A=
NM_000089.4:c.378+26A= MANE Select NP_000080.2:n.378+26A=
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