Canonical Allele Identifier: CA349843650
Gene: COL3A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189868706A>C (hg19) chr2:g.189003980A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189003980A>C , CM000664.2:g.189003980A>C GRCh38
NC_000002.11:g.189868706A>C , CM000664.1:g.189868706A>C GRCh37
NC_000002.10:g.189576951A>C NCBI36
NG_007404.1:g.34608A>C , LRG_3:g.34608A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000450867.2:c.2563-2A>C ENSP00000415346.2:n.2563-2A>C
ENST00000304636.9:c.2662-2A>C MANE Select ENSP00000304408.4:n.2662-2A>C
ENST00000304636.7:c.2662-2A>C ENSP00000304408.3:n.2662-2A>C
ENST00000317840.9:c.2527+944A>C ENSP00000315243.6:n.2527+944A>C
NM_000090.3:c.2662-2A>C , LRG_3t1:c.2662-2A>C NP_000081.1:n.2662-2A>C
NM_000090.4:c.2662-2A>C MANE Select NP_000081.2:n.2662-2A>C
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