Canonical Allele Identifier: CA349844383
Gene: COL3A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189868982G>C (hg19) chr2:g.189004256G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189004256G>C , CM000664.2:g.189004256G>C GRCh38
NC_000002.11:g.189868982G>C , CM000664.1:g.189868982G>C GRCh37
NC_000002.10:g.189577227G>C NCBI36
NG_007404.1:g.34884G>C , LRG_3:g.34884G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000450867.2:c.2725-1G>C ENSP00000415346.2:n.2725-1G>C
ENST00000304636.9:c.2824-1G>C MANE Select ENSP00000304408.4:n.2824-1G>C
ENST00000304636.7:c.2824-1G>C ENSP00000304408.3:n.2824-1G>C
ENST00000317840.9:c.2527+1220G>C ENSP00000315243.6:n.2527+1220G>C
NM_000090.3:c.2824-1G>C , LRG_3t1:c.2824-1G>C NP_000081.1:n.2824-1G>C
NM_000090.4:c.2824-1G>C MANE Select NP_000081.2:n.2824-1G>C
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