Canonical Allele Identifier: CA62597390
Gene: COL3A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1403090
dbSNP Id: rs373963384

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188996178C>G , CM000664.2:g.188996178C>G GRCh38
NC_000002.11:g.189860904C>G , CM000664.1:g.189860904C>G GRCh37
NC_000002.10:g.189569149C>G NCBI36
NG_007404.1:g.26806C>G , LRG_3:g.26806C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000450867.2:c.1563C>G ENSP00000415346.2:p.Pro521=
ENST00000304636.9:c.1662C>G MANE Select ENSP00000304408.4:p.Pro554=
ENST00000304636.7:c.1662C>G ENSP00000304408.3:p.Pro554=
ENST00000317840.9:c.1662C>G ENSP00000315243.6:p.Pro554=
NM_000090.3:c.1662C>G , LRG_3t1:c.1662C>G NP_000081.1:p.Pro554=
NM_000090.4:c.1662C>G MANE Select NP_000081.2:p.Pro554=