Canonical Allele Identifier: CA1726792153
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404586G= , CM000669.2:g.94404586G= GRCh38
NC_000007.13:g.94033898G= , CM000669.1:g.94033898G= GRCh37
NC_000007.12:g.93871834G= NCBI36
NG_007405.1:g.15026G= , LRG_2:g.15026G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.310G= MANE Select ENSP00000297268.6:p.Ala104=
ENST00000297268.10:c.310G= ENSP00000297268.6:p.Ala104=
ENST00000620463.1:c.304G= ENSP00000477719.1:p.Ala102=
NM_000089.3:c.310G= , LRG_2t1:c.310G= NP_000080.2:p.Ala104=
NM_000089.4:c.310G= MANE Select NP_000080.2:p.Ala104=