Canonical Allele Identifier: CA844000829
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1489540151
gnomAD v4: 7-94422836-G-A
MyVariant Identifiers: chr7:g.94052148G>A (hg19) chr7:g.94422836G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94422836G>A , CM000669.2:g.94422836G>A GRCh38
NC_000007.13:g.94052148G>A , CM000669.1:g.94052148G>A GRCh37
NC_000007.12:g.93890084G>A NCBI36
NG_007405.1:g.33276G>A , LRG_2:g.33276G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.2404-121G>A MANE Select ENSP00000297268.6:n.2404-121G>A
ENST00000297268.10:c.2404-121G>A ENSP00000297268.6:n.2404-121G>A
ENST00000481570.5:n.366G>A
ENST00000497316.5:n.801-121G>A
ENST00000620463.1:c.2398-121G>A ENSP00000477719.1:n.2398-121G>A
NM_000089.3:c.2404-121G>A , LRG_2t1:c.2404-121G>A NP_000080.2:n.2404-121G>A
NM_000089.4:c.2404-121G>A MANE Select NP_000080.2:n.2404-121G>A
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