Canonical Allele Identifier: CA1726763461
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94415269G= , CM000669.2:g.94415269G= GRCh38
NC_000007.13:g.94044581G= , CM000669.1:g.94044581G= GRCh37
NC_000007.12:g.93882517G= NCBI36
NG_007405.1:g.25709G= , LRG_2:g.25709G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.1763G= MANE Select ENSP00000297268.6:p.Arg588=
ENST00000297268.10:c.1763G= ENSP00000297268.6:p.Arg588=
ENST00000473573.5:n.100G=
ENST00000488298.5:n.187G=
ENST00000620463.1:c.1757G= ENSP00000477719.1:p.Arg586=
NM_000089.3:c.1763G= , LRG_2t1:c.1763G= NP_000080.2:p.Arg588=
NM_000089.4:c.1763G= MANE Select NP_000080.2:p.Arg588=