Canonical Allele Identifier: CA430466684
Gene: COL3A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189849682A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188984956A>T , CM000664.2:g.188984956A>T GRCh38
NC_000002.11:g.189849682A>T , CM000664.1:g.189849682A>T GRCh37
NC_000002.10:g.189557927A>T NCBI36
NG_007404.1:g.15584A>T , LRG_3:g.15584A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000450867.2:c.276A>T ENSP00000415346.2:p.Pro92=
ENST00000304636.9:c.276A>T MANE Select ENSP00000304408.4:p.Pro92=
ENST00000304636.7:c.276A>T ENSP00000304408.3:p.Pro92=
ENST00000317840.9:c.276A>T ENSP00000315243.6:p.Pro92=
ENST00000470167.1:n.372A>T
NM_000090.3:c.276A>T , LRG_3t1:c.276A>T NP_000081.1:p.Pro92=
NM_000090.4:c.276A>T MANE Select NP_000081.2:p.Pro92=
Search 100 bp 5'
Search 100 bp 3'