Canonical Allele Identifier: CA430308950
Gene: COL3A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189853327A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188988601A>C , CM000664.2:g.188988601A>C GRCh38
NC_000002.11:g.189853327A>C , CM000664.1:g.189853327A>C GRCh37
NC_000002.10:g.189561572A>C NCBI36
NG_007404.1:g.19229A>C , LRG_3:g.19229A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000450867.2:c.594A>C ENSP00000415346.2:p.Gly198=
ENST00000304636.9:c.594A>C MANE Select ENSP00000304408.4:p.Gly198=
ENST00000304636.7:c.594A>C ENSP00000304408.3:p.Gly198=
ENST00000317840.9:c.594A>C ENSP00000315243.6:p.Gly198=
NM_000090.3:c.594A>C , LRG_3t1:c.594A>C NP_000081.1:p.Gly198=
NM_000090.4:c.594A>C MANE Select NP_000081.2:p.Gly198=