Canonical Allele Identifier: CA349842808
Gene: COL3A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1339754
ClinVar RCV Id: RCV001825142 RCV002542768
dbSNP Id: rs2153503381
MyVariant Identifiers: chr2:g.189867735G>C (hg19) chr2:g.189003009G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189003009G>C , CM000664.2:g.189003009G>C GRCh38
NC_000002.11:g.189867735G>C , CM000664.1:g.189867735G>C GRCh37
NC_000002.10:g.189575980G>C NCBI36
NG_007404.1:g.33637G>C , LRG_3:g.33637G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000450867.2:c.2401G>C ENSP00000415346.2:p.Gly801Arg
ENST00000304636.9:c.2500G>C MANE Select ENSP00000304408.4:p.Gly834Arg
ENST00000304636.7:c.2500G>C ENSP00000304408.3:p.Gly834Arg
ENST00000317840.9:c.2500G>C ENSP00000315243.6:p.Gly834Arg
NM_000090.3:c.2500G>C , LRG_3t1:c.2500G>C NP_000081.1:p.Gly834Arg
NM_000090.4:c.2500G>C MANE Select NP_000081.2:p.Gly834Arg
Search 100 bp 5'
Search 100 bp 3'