Canonical Allele Identifier: CA007568
Gene: COL3A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 101131
ClinVar RCV Id: RCV000087368
dbSNP Id: rs121912919

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188991678G>A , CM000664.2:g.188991678G>A GRCh38
NC_000002.11:g.189856404G>A , CM000664.1:g.189856404G>A GRCh37
NC_000002.10:g.189564649G>A NCBI36
NG_007404.1:g.22306G>A , LRG_3:g.22306G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000450867.2:c.907G>A ENSP00000415346.2:p.Gly303Arg
ENST00000304636.9:c.907G>A MANE Select ENSP00000304408.4:p.Gly303Arg
ENST00000304636.7:c.907G>A ENSP00000304408.3:p.Gly303Arg
ENST00000317840.9:c.907G>A ENSP00000315243.6:p.Gly303Arg
ENST00000450867.1:c.5G>A
NM_000090.3:c.907G>A , LRG_3t1:c.907G>A NP_000081.1:p.Gly303Arg
NM_000090.4:c.907G>A MANE Select NP_000081.2:p.Gly303Arg