Canonical Allele Identifier: CA368220291
Gene: COL1A2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.94037531G>C (hg19) chr7:g.94408219G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94408219G>C , CM000669.2:g.94408219G>C GRCh38
NC_000007.13:g.94037531G>C , CM000669.1:g.94037531G>C GRCh37
NC_000007.12:g.93875467G>C NCBI36
NG_007405.1:g.18659G>C , LRG_2:g.18659G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000297268.11:c.676G>C MANE Select ENSP00000297268.6:p.Gly226Arg
ENST00000297268.10:c.676G>C ENSP00000297268.6:p.Gly226Arg
ENST00000620463.1:c.670G>C ENSP00000477719.1:p.Gly224Arg
NM_000089.3:c.676G>C , LRG_2t1:c.676G>C NP_000080.2:p.Gly226Arg
NM_000089.4:c.676G>C MANE Select NP_000080.2:p.Gly226Arg
Search 100 bp 5'
Search 100 bp 3'