Canonical Allele Identifier: CA162940267
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs904266581
gnomAD v3: 7-94426205-T-C
gnomAD v4: 7-94426205-T-C
MyVariant Identifiers: chr7:g.94055517T>C (hg19) chr7:g.94426205T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94426205T>C , CM000669.2:g.94426205T>C GRCh38
NC_000007.13:g.94055517T>C , CM000669.1:g.94055517T>C GRCh37
NC_000007.12:g.93893453T>C NCBI36
NG_007405.1:g.36645T>C , LRG_2:g.36645T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2997+154T>C MANE Select ENSP00000297268.6:n.2997+154T>C
ENST00000297268.10:c.2997+154T>C ENSP00000297268.6:n.2997+154T>C
ENST00000478215.1:n.556+154T>C
ENST00000481570.5:n.2970+154T>C
ENST00000620463.1:c.2991+154T>C ENSP00000477719.1:n.2991+154T>C
NM_000089.3:c.2997+154T>C , LRG_2t1:c.2997+154T>C NP_000080.2:n.2997+154T>C
NM_000089.4:c.2997+154T>C MANE Select NP_000080.2:n.2997+154T>C
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