Canonical Allele Identifier: CA1726782500
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94426023C= , CM000669.2:g.94426023C= GRCh38
NC_000007.13:g.94055335C= , CM000669.1:g.94055335C= GRCh37
NC_000007.12:g.93893271C= NCBI36
NG_007405.1:g.36463C= , LRG_2:g.36463C=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2969C= MANE Select ENSP00000297268.6:p.Ala990=
ENST00000297268.10:c.2969C= ENSP00000297268.6:p.Ala990=
ENST00000478215.1:n.528C=
ENST00000481570.5:n.2942C=
ENST00000620463.1:c.2963C= ENSP00000477719.1:p.Ala988=
NM_000089.3:c.2969C= , LRG_2t1:c.2969C= NP_000080.2:p.Ala990=
NM_000089.4:c.2969C= MANE Select NP_000080.2:p.Ala990=