Canonical Allele Identifier: CA10629666

Gene: COL1A2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.94417836G>A , CM000669.2:g.94417836G>A	GRCh38
NC_000007.13:g.94047148G>A , CM000669.1:g.94047148G>A	GRCh37
NC_000007.12:g.93885084G>A	NCBI36
NG_007405.1:g.28276G>A , LRG_2:g.28276G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297268.11:c.1971+5G>A MANE Select	ENSP00000297268.6:n.1971+5G>A
ENST00000297268.10:c.1971+5G>A	ENSP00000297268.6:n.1971+5G>A
ENST00000461525.5:n.60+5G>A
ENST00000473573.5:n.308+5G>A
ENST00000497316.5:n.368+5G>A
ENST00000620463.1:c.1965+5G>A	ENSP00000477719.1:n.1965+5G>A
NM_000089.3:c.1971+5G>A , LRG_2t1:c.1971+5G>A	NP_000080.2:n.1971+5G>A
NM_000089.4:c.1971+5G>A MANE Select	NP_000080.2:n.1971+5G>A