Canonical Allele Identifier: CA349844800
Gene: COL3A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189870142C>G (hg19) chr2:g.189005416C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189005416C>G , CM000664.2:g.189005416C>G GRCh38
NC_000002.11:g.189870142C>G , CM000664.1:g.189870142C>G GRCh37
NC_000002.10:g.189578387C>G NCBI36
NG_007404.1:g.36044C>G , LRG_3:g.36044C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000450867.2:c.2899C>G ENSP00000415346.2:p.Leu967Val
ENST00000304636.9:c.2998C>G MANE Select ENSP00000304408.4:p.Leu1000Val
ENST00000304636.7:c.2998C>G ENSP00000304408.3:p.Leu1000Val
ENST00000317840.9:c.2527+2380C>G ENSP00000315243.6:n.2527+2380C>G
NM_000090.3:c.2998C>G , LRG_3t1:c.2998C>G NP_000081.1:p.Leu1000Val
NM_000090.4:c.2998C>G MANE Select NP_000081.2:p.Leu1000Val
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