Canonical Allele Identifier: CA844003776

Gene: COL1A2

Linked Data

• dbSNP Id: rs1237409262
• MyVariant Identifiers: chr7:g.94055919del (hg19) ; chr7:g.94426607del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.94426607del , CM000669.2:g.94426607del	GRCh38
NC_000007.13:g.94055919del , CM000669.1:g.94055919del	GRCh37
NC_000007.12:g.93893855del	NCBI36
NG_007405.1:g.37047del , LRG_2:g.37047del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297268.11:c.3105+77del MANE Select	ENSP00000297268.6:n.3105+77del
ENST00000297268.10:c.3105+77del	ENSP00000297268.6:n.3105+77del
ENST00000478215.1:n.741del
ENST00000481570.5:n.3155del
ENST00000488121.1:n.21+77del
ENST00000620463.1:c.3099+77del	ENSP00000477719.1:n.3099+77del
NM_000089.3:c.3105+77del , LRG_2t1:c.3105+77del	NP_000080.2:n.3105+77del
NM_000089.4:c.3105+77del MANE Select	NP_000080.2:n.3105+77del