Canonical Allele Identifier: CA162940351
Gene: COL1A2 HGNC NCBI

Linked Data

dbSNP Id: rs72659320
MyVariant Identifiers: chr7:g.94055780G>C (hg19) chr7:g.94426468G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94426468G>C , CM000669.2:g.94426468G>C GRCh38
NC_000007.13:g.94055780G>C , CM000669.1:g.94055780G>C GRCh37
NC_000007.12:g.93893716G>C NCBI36
NG_007405.1:g.36908G>C , LRG_2:g.36908G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.3043G>C MANE Select ENSP00000297268.6:p.Gly1015Arg
ENST00000297268.10:c.3043G>C ENSP00000297268.6:p.Gly1015Arg
ENST00000478215.1:n.602G>C
ENST00000481570.5:n.3016G>C
ENST00000620463.1:c.3037G>C ENSP00000477719.1:p.Gly1013Arg
NM_000089.3:c.3043G>C , LRG_2t1:c.3043G>C NP_000080.2:p.Gly1015Arg
NM_000089.4:c.3043G>C MANE Select NP_000080.2:p.Gly1015Arg
Search 100 bp 5'
Search 100 bp 3'