Canonical Allele Identifier: CA349843687
Gene: COL3A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1421209
ClinVar RCV Id: RCV001943739
dbSNP Id: rs794728053
gnomAD v4: 2-189003988-C-G
MyVariant Identifiers: chr2:g.189868714C>G (hg19) chr2:g.189003988C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189003988C>G , CM000664.2:g.189003988C>G GRCh38
NC_000002.11:g.189868714C>G , CM000664.1:g.189868714C>G GRCh37
NC_000002.10:g.189576959C>G NCBI36
NG_007404.1:g.34616C>G , LRG_3:g.34616C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000450867.2:c.2569C>G ENSP00000415346.2:p.Pro857Ala
ENST00000304636.9:c.2668C>G MANE Select ENSP00000304408.4:p.Pro890Ala
ENST00000304636.7:c.2668C>G ENSP00000304408.3:p.Pro890Ala
ENST00000317840.9:c.2527+952C>G ENSP00000315243.6:n.2527+952C>G
NM_000090.3:c.2668C>G , LRG_3t1:c.2668C>G NP_000081.1:p.Pro890Ala
NM_000090.4:c.2668C>G MANE Select NP_000081.2:p.Pro890Ala
Search 100 bp 5'
Search 100 bp 3'