Canonical Allele Identifier: CA844000790
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1209285255
MyVariant Identifiers: chr7:g.94052086A>C (hg19) chr7:g.94422774A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94422774A>C , CM000669.2:g.94422774A>C GRCh38
NC_000007.13:g.94052086A>C , CM000669.1:g.94052086A>C GRCh37
NC_000007.12:g.93890022A>C NCBI36
NG_007405.1:g.33214A>C , LRG_2:g.33214A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2404-183A>C MANE Select ENSP00000297268.6:n.2404-183A>C
ENST00000297268.10:c.2404-183A>C ENSP00000297268.6:n.2404-183A>C
ENST00000481570.5:n.304A>C
ENST00000497316.5:n.801-183A>C
ENST00000620463.1:c.2398-183A>C ENSP00000477719.1:n.2398-183A>C
NM_000089.3:c.2404-183A>C , LRG_2t1:c.2404-183A>C NP_000080.2:n.2404-183A>C
NM_000089.4:c.2404-183A>C MANE Select NP_000080.2:n.2404-183A>C
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