Canonical Allele Identifier: CA62593519
Gene: COL3A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2064181
ClinVar RCV Id: RCV002943272
dbSNP Id: rs944459180

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188992241C>T , CM000664.2:g.188992241C>T GRCh38
NC_000002.11:g.189856967C>T , CM000664.1:g.189856967C>T GRCh37
NC_000002.10:g.189565212C>T NCBI36
NG_007404.1:g.22869C>T , LRG_3:g.22869C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000450867.2:c.996+13C>T ENSP00000415346.2:n.996+13C>T
ENST00000304636.9:c.996+13C>T MANE Select ENSP00000304408.4:n.996+13C>T
ENST00000304636.7:c.996+13C>T ENSP00000304408.3:n.996+13C>T
ENST00000317840.9:c.996+13C>T ENSP00000315243.6:n.996+13C>T
ENST00000450867.1:c.94+13C>T
NM_000090.3:c.996+13C>T , LRG_3t1:c.996+13C>T NP_000081.1:n.996+13C>T
NM_000090.4:c.996+13C>T MANE Select NP_000081.2:n.996+13C>T