Canonical Allele Identifier: CA1726792197
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404695C= , CM000669.2:g.94404695C= GRCh38
NC_000007.13:g.94034007C= , CM000669.1:g.94034007C= GRCh37
NC_000007.12:g.93871943C= NCBI36
NG_007405.1:g.15135C= , LRG_2:g.15135C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.327C= MANE Select ENSP00000297268.6:p.Gly109=
ENST00000297268.10:c.327C= ENSP00000297268.6:p.Gly109=
ENST00000620463.1:c.321C= ENSP00000477719.1:p.Gly107=
NM_000089.3:c.327C= , LRG_2t1:c.327C= NP_000080.2:p.Gly109=
NM_000089.4:c.327C= MANE Select NP_000080.2:p.Gly109=