Canonical Allele Identifier: CA1726792146
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404575G= , CM000669.2:g.94404575G= GRCh38
NC_000007.13:g.94033887G= , CM000669.1:g.94033887G= GRCh37
NC_000007.12:g.93871823G= NCBI36
NG_007405.1:g.15015G= , LRG_2:g.15015G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.299G= MANE Select ENSP00000297268.6:p.Gly100=
ENST00000297268.10:c.299G= ENSP00000297268.6:p.Gly100=
ENST00000620463.1:c.293G= ENSP00000477719.1:p.Gly98=
NM_000089.3:c.299G= , LRG_2t1:c.299G= NP_000080.2:p.Gly100=
NM_000089.4:c.299G= MANE Select NP_000080.2:p.Gly100=