Canonical Allele Identifier: CA456487030
Gene: COL1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94033879A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404567A>T , CM000669.2:g.94404567A>T GRCh38
NC_000007.13:g.94033879A>T , CM000669.1:g.94033879A>T GRCh37
NC_000007.12:g.93871815A>T NCBI36
NG_007405.1:g.15007A>T , LRG_2:g.15007A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.291A>T MANE Select ENSP00000297268.6:p.Gly97=
ENST00000297268.10:c.291A>T ENSP00000297268.6:p.Gly97=
ENST00000620463.1:c.285A>T ENSP00000477719.1:p.Gly95=
NM_000089.3:c.291A>T , LRG_2t1:c.291A>T NP_000080.2:p.Gly97=
NM_000089.4:c.291A>T MANE Select NP_000080.2:p.Gly97=
Search 100 bp 5'
Search 100 bp 3'