Canonical Allele Identifier: CA2573133084
Gene: COL3A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1585454
ClinVar RCV Id: RCV002095418
dbSNP Id: rs1243909889

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188996111C>G , CM000664.2:g.188996111C>G GRCh38
NC_000002.11:g.189860837C>G , CM000664.1:g.189860837C>G GRCh37
NC_000002.10:g.189569082C>G NCBI36
NG_007404.1:g.26739C>G , LRG_3:g.26739C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000450867.2:c.1510-14C>G ENSP00000415346.2:n.1510-14C>G
ENST00000304636.9:c.1609-14C>G MANE Select ENSP00000304408.4:n.1609-14C>G
ENST00000304636.7:c.1609-14C>G ENSP00000304408.3:n.1609-14C>G
ENST00000317840.9:c.1609-14C>G ENSP00000315243.6:n.1609-14C>G
NM_000090.3:c.1609-14C>G , LRG_3t1:c.1609-14C>G NP_000081.1:n.1609-14C>G
NM_000090.4:c.1609-14C>G MANE Select NP_000081.2:n.1609-14C>G