Canonical Allele Identifier: CA1726792256
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404855G= , CM000669.2:g.94404855G= GRCh38
NC_000007.13:g.94034167G= , CM000669.1:g.94034167G= GRCh37
NC_000007.12:g.93872103G= NCBI36
NG_007405.1:g.15295G= , LRG_2:g.15295G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.395G= MANE Select ENSP00000297268.6:p.Arg132=
ENST00000297268.10:c.395G= ENSP00000297268.6:p.Arg132=
ENST00000620463.1:c.389G= ENSP00000477719.1:p.Arg130=
NM_000089.3:c.395G= , LRG_2t1:c.395G= NP_000080.2:p.Arg132=
NM_000089.4:c.395G= MANE Select NP_000080.2:p.Arg132=