Canonical Allele Identifier: CA1726792264
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404868C= , CM000669.2:g.94404868C= GRCh38
NC_000007.13:g.94034180C= , CM000669.1:g.94034180C= GRCh37
NC_000007.12:g.93872116C= NCBI36
NG_007405.1:g.15308C= , LRG_2:g.15308C=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.408C= MANE Select ENSP00000297268.6:p.Gly136=
ENST00000297268.10:c.408C= ENSP00000297268.6:p.Gly136=
ENST00000620463.1:c.402C= ENSP00000477719.1:p.Gly134=
NM_000089.3:c.408C= , LRG_2t1:c.408C= NP_000080.2:p.Gly136=
NM_000089.4:c.408C= MANE Select NP_000080.2:p.Gly136=