Canonical Allele Identifier: CA368223982
Gene: COL1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94052329C>A (hg19) chr7:g.94423017C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94423017C>A , CM000669.2:g.94423017C>A GRCh38
NC_000007.13:g.94052329C>A , CM000669.1:g.94052329C>A GRCh37
NC_000007.12:g.93890265C>A NCBI36
NG_007405.1:g.33457C>A , LRG_2:g.33457C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.2464C>A MANE Select ENSP00000297268.6:p.Arg822Ser
ENST00000297268.10:c.2464C>A ENSP00000297268.6:p.Arg822Ser
ENST00000481570.5:n.547C>A
ENST00000497316.5:n.861C>A
ENST00000620463.1:c.2458C>A ENSP00000477719.1:p.Arg820Ser
NM_000089.3:c.2464C>A , LRG_2t1:c.2464C>A NP_000080.2:p.Arg822Ser
NM_000089.4:c.2464C>A MANE Select NP_000080.2:p.Arg822Ser
Search 100 bp 5'
Search 100 bp 3'