Canonical Allele Identifier: CA430309201
Gene: COL3A1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.189856412T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.188991686T>C , CM000664.2:g.188991686T>C GRCh38
NC_000002.11:g.189856412T>C , CM000664.1:g.189856412T>C GRCh37
NC_000002.10:g.189564657T>C NCBI36
NG_007404.1:g.22314T>C , LRG_3:g.22314T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000450867.2:c.915T>C ENSP00000415346.2:p.Pro305=
ENST00000304636.9:c.915T>C MANE Select ENSP00000304408.4:p.Pro305=
ENST00000304636.7:c.915T>C ENSP00000304408.3:p.Pro305=
ENST00000317840.9:c.915T>C ENSP00000315243.6:p.Pro305=
ENST00000450867.1:c.13T>C
NM_000090.3:c.915T>C , LRG_3t1:c.915T>C NP_000081.1:p.Pro305=
NM_000090.4:c.915T>C MANE Select NP_000081.2:p.Pro305=