Canonical Allele Identifier: CA1726763425
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94415263G= , CM000669.2:g.94415263G= GRCh38
NC_000007.13:g.94044575G= , CM000669.1:g.94044575G= GRCh37
NC_000007.12:g.93882511G= NCBI36
NG_007405.1:g.25703G= , LRG_2:g.25703G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.1757G= MANE Select ENSP00000297268.6:p.Gly586=
ENST00000297268.10:c.1757G= ENSP00000297268.6:p.Gly586=
ENST00000473573.5:n.94G=
ENST00000488298.5:n.181G=
ENST00000620463.1:c.1751G= ENSP00000477719.1:p.Gly584=
NM_000089.3:c.1757G= , LRG_2t1:c.1757G= NP_000080.2:p.Gly586=
NM_000089.4:c.1757G= MANE Select NP_000080.2:p.Gly586=