Canonical Allele Identifier: CA162919498
Gene: COL1A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 425661
ClinVar RCV Id: RCV000490709 RCV001851298
dbSNP Id: rs72656386
MyVariant Identifiers: chr7:g.94038635G>A (hg19) chr7:g.94409323G>A (hg38)
PubMed: PMID:25944380
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94409323G>A , CM000669.2:g.94409323G>A GRCh38
NC_000007.13:g.94038635G>A , CM000669.1:g.94038635G>A GRCh37
NC_000007.12:g.93876571G>A NCBI36
NG_007405.1:g.19763G>A , LRG_2:g.19763G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.794G>A MANE Select ENSP00000297268.6:p.Gly265Asp
ENST00000297268.10:c.794G>A ENSP00000297268.6:p.Gly265Asp
ENST00000620463.1:c.788G>A ENSP00000477719.1:p.Gly263Asp
NM_000089.3:c.794G>A , LRG_2t1:c.794G>A NP_000080.2:p.Gly265Asp
NM_000089.4:c.794G>A MANE Select NP_000080.2:p.Gly265Asp
Search 100 bp 5'
Search 100 bp 3'