Canonical Allele Identifier: CA456489573
Gene: COL1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94052298T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94422986T>A , CM000669.2:g.94422986T>A GRCh38
NC_000007.13:g.94052298T>A , CM000669.1:g.94052298T>A GRCh37
NC_000007.12:g.93890234T>A NCBI36
NG_007405.1:g.33426T>A , LRG_2:g.33426T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2433T>A MANE Select ENSP00000297268.6:p.Gly811=
ENST00000297268.10:c.2433T>A ENSP00000297268.6:p.Gly811=
ENST00000481570.5:n.516T>A
ENST00000497316.5:n.830T>A
ENST00000620463.1:c.2427T>A ENSP00000477719.1:p.Gly809=
NM_000089.3:c.2433T>A , LRG_2t1:c.2433T>A NP_000080.2:p.Gly811=
NM_000089.4:c.2433T>A MANE Select NP_000080.2:p.Gly811=
Search 100 bp 5'
Search 100 bp 3'