Canonical Allele Identifier: CA349844817
Gene: COL3A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189870152T>A (hg19) chr2:g.189005426T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189005426T>A , CM000664.2:g.189005426T>A GRCh38
NC_000002.11:g.189870152T>A , CM000664.1:g.189870152T>A GRCh37
NC_000002.10:g.189578397T>A NCBI36
NG_007404.1:g.36054T>A , LRG_3:g.36054T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000450867.2:c.2909T>A ENSP00000415346.2:p.Leu970Gln
ENST00000304636.9:c.3008T>A MANE Select ENSP00000304408.4:p.Leu1003Gln
ENST00000304636.7:c.3008T>A ENSP00000304408.3:p.Leu1003Gln
ENST00000317840.9:c.2527+2390T>A ENSP00000315243.6:n.2527+2390T>A
NM_000090.3:c.3008T>A , LRG_3t1:c.3008T>A NP_000081.1:p.Leu1003Gln
NM_000090.4:c.3008T>A MANE Select NP_000081.2:p.Leu1003Gln
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