Canonical Allele Identifier: CA1726750479
Gene: COL1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94409302G= , CM000669.2:g.94409302G= GRCh38
NC_000007.13:g.94038614G= , CM000669.1:g.94038614G= GRCh37
NC_000007.12:g.93876550G= NCBI36
NG_007405.1:g.19742G= , LRG_2:g.19742G=

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.793-20G= MANE Select ENSP00000297268.6:n.793-20G=
ENST00000297268.10:c.793-20G= ENSP00000297268.6:n.793-20G=
ENST00000620463.1:c.787-20G= ENSP00000477719.1:n.787-20G=
NM_000089.3:c.793-20G= , LRG_2t1:c.793-20G= NP_000080.2:n.793-20G=
NM_000089.4:c.793-20G= MANE Select NP_000080.2:n.793-20G=