Canonical Allele Identifier: CA1726783419
Gene: COL1A2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94426576C= , CM000669.2:g.94426576C= GRCh38
NC_000007.13:g.94055888C= , CM000669.1:g.94055888C= GRCh37
NC_000007.12:g.93893824C= NCBI36
NG_007405.1:g.37016C= , LRG_2:g.37016C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.3105+46C= MANE Select ENSP00000297268.6:n.3105+46C=
ENST00000297268.10:c.3105+46C= ENSP00000297268.6:n.3105+46C=
ENST00000478215.1:n.710C=
ENST00000481570.5:n.3124C=
ENST00000488121.1:n.21+46C=
ENST00000620463.1:c.3099+46C= ENSP00000477719.1:n.3099+46C=
NM_000089.3:c.3105+46C= , LRG_2t1:c.3105+46C= NP_000080.2:n.3105+46C=
NM_000089.4:c.3105+46C= MANE Select NP_000080.2:n.3105+46C=
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