Canonical Allele Identifier: CA430310572
Gene: COL3A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2586764
ClinVar RCV Id: RCV003341830
dbSNP Id: rs746947080
gnomAD v4: 2-188999371-C-A
MyVariant Identifiers: chr2:g.189864097C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188999371C>A , CM000664.2:g.188999371C>A GRCh38
NC_000002.11:g.189864097C>A , CM000664.1:g.189864097C>A GRCh37
NC_000002.10:g.189572342C>A NCBI36
NG_007404.1:g.29999C>A , LRG_3:g.29999C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000450867.2:c.2010C>A ENSP00000415346.2:p.Pro670=
ENST00000304636.9:c.2109C>A MANE Select ENSP00000304408.4:p.Pro703=
ENST00000304636.7:c.2109C>A ENSP00000304408.3:p.Pro703=
ENST00000317840.9:c.2109C>A ENSP00000315243.6:p.Pro703=
NM_000090.3:c.2109C>A , LRG_3t1:c.2109C>A NP_000081.1:p.Pro703=
NM_000090.4:c.2109C>A MANE Select NP_000081.2:p.Pro703=
Search 100 bp 5'
Search 100 bp 3'