Canonical Allele Identifier: CA005666
Gene: COL3A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 101139
ClinVar RCV Id: RCV000087376 RCV002433595
dbSNP Id: rs587779450
MyVariant Identifiers: chr2:g.189868817G>A (hg19) chr2:g.189004091G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189004091G>A , CM000664.2:g.189004091G>A GRCh38
NC_000002.11:g.189868817G>A , CM000664.1:g.189868817G>A GRCh37
NC_000002.10:g.189577062G>A NCBI36
NG_007404.1:g.34719G>A , LRG_3:g.34719G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000450867.2:c.2672G>A ENSP00000415346.2:p.Gly891Asp
ENST00000304636.9:c.2771G>A MANE Select ENSP00000304408.4:p.Gly924Asp
ENST00000304636.7:c.2771G>A ENSP00000304408.3:p.Gly924Asp
ENST00000317840.9:c.2527+1055G>A ENSP00000315243.6:n.2527+1055G>A
NM_000090.3:c.2771G>A , LRG_3t1:c.2771G>A NP_000081.1:p.Gly924Asp
NM_000090.4:c.2771G>A MANE Select NP_000081.2:p.Gly924Asp
Search 100 bp 5'
Search 100 bp 3'