Canonical Allele Identifier: CA162913932
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs772225332
gnomAD v4: 7-94404511-A-G
MyVariant Identifiers: chr7:g.94033823A>G (hg19) chr7:g.94404511A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94404511A>G , CM000669.2:g.94404511A>G GRCh38
NC_000007.13:g.94033823A>G , CM000669.1:g.94033823A>G GRCh37
NC_000007.12:g.93871759A>G NCBI36
NG_007405.1:g.14951A>G , LRG_2:g.14951A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.280-45A>G MANE Select ENSP00000297268.6:n.280-45A>G
ENST00000297268.10:c.280-45A>G ENSP00000297268.6:n.280-45A>G
ENST00000620463.1:c.274-45A>G ENSP00000477719.1:n.274-45A>G
NM_000089.3:c.280-45A>G , LRG_2t1:c.280-45A>G NP_000080.2:n.280-45A>G
NM_000089.4:c.280-45A>G MANE Select NP_000080.2:n.280-45A>G
Search 100 bp 5'
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