Canonical Allele Identifier: CA430310915
Gene: COL3A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189866155A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.189001429A>T , CM000664.2:g.189001429A>T GRCh38
NC_000002.11:g.189866155A>T , CM000664.1:g.189866155A>T GRCh37
NC_000002.10:g.189574400A>T NCBI36
NG_007404.1:g.32057A>T , LRG_3:g.32057A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000450867.2:c.2217A>T ENSP00000415346.2:p.Pro739=
ENST00000304636.9:c.2316A>T MANE Select ENSP00000304408.4:p.Pro772=
ENST00000304636.7:c.2316A>T ENSP00000304408.3:p.Pro772=
ENST00000317840.9:c.2316A>T ENSP00000315243.6:p.Pro772=
NM_000090.3:c.2316A>T , LRG_3t1:c.2316A>T NP_000081.1:p.Pro772=
NM_000090.4:c.2316A>T MANE Select NP_000081.2:p.Pro772=