Canonical Allele Identifier: CA368223862
Gene: COL1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94052267A>G (hg19) chr7:g.94422955A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94422955A>G , CM000669.2:g.94422955A>G GRCh38
NC_000007.13:g.94052267A>G , CM000669.1:g.94052267A>G GRCh37
NC_000007.12:g.93890203A>G NCBI36
NG_007405.1:g.33395A>G , LRG_2:g.33395A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2404-2A>G MANE Select ENSP00000297268.6:n.2404-2A>G
ENST00000297268.10:c.2404-2A>G ENSP00000297268.6:n.2404-2A>G
ENST00000481570.5:n.485A>G
ENST00000497316.5:n.801-2A>G
ENST00000620463.1:c.2398-2A>G ENSP00000477719.1:n.2398-2A>G
NM_000089.3:c.2404-2A>G , LRG_2t1:c.2404-2A>G NP_000080.2:n.2404-2A>G
NM_000089.4:c.2404-2A>G MANE Select NP_000080.2:n.2404-2A>G
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