Canonical Allele Identifier: CA368220543
Gene: COL1A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1457226
ClinVar RCV Id: RCV001953647 RCV003401970
dbSNP Id: rs72656386
MyVariant Identifiers: chr7:g.94038635G>T (hg19) chr7:g.94409323G>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.794G>T MANE Select ENSP00000297268.6:p.Gly265Val
ENST00000297268.10:c.794G>T ENSP00000297268.6:p.Gly265Val
ENST00000620463.1:c.788G>T ENSP00000477719.1:p.Gly263Val
NM_000089.3:c.794G>T , LRG_2t1:c.794G>T NP_000080.2:p.Gly265Val
NM_000089.4:c.794G>T MANE Select NP_000080.2:p.Gly265Val
Search 100 bp 5'
Search 100 bp 3'