Canonical Allele Identifier: CA368221811
Gene: COL1A2 HGNC NCBI
MyVariant.info:
GRCh38 chr7:g.94412593G>C
GRCh37 chr7:g.94041905G>C
Revel Score:
ENST00000297268 (MANE Select) 0.978
ENST00000545487 0.978
ClinVar RCV:
RCV002277774
ClinVar Variation:
1701990
dbSNP:
121912906
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94412593G>C , CM000669.2:g.94412593G>C GRCh38
NC_000007.13:g.94041905G>C , CM000669.1:g.94041905G>C GRCh37
NC_000007.12:g.93879841G>C NCBI36
NG_007405.1:g.23033G>C , LRG_2:g.23033G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000297268.11:c.1414G>C MANE Select ENSP00000297268.6:p.Gly472Arg
ENST00000297268.10:c.1414G>C ENSP00000297268.6:p.Gly472Arg
ENST00000620463.1:c.1408G>C ENSP00000477719.1:p.Gly470Arg
NM_000089.3:c.1414G>C , LRG_2t1:c.1414G>C NP_000080.2:p.Gly472Arg
NM_000089.4:c.1414G>C MANE Select NP_000080.2:p.Gly472Arg
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