Canonical Allele Identifier: CA425339856
Gene: MATN3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.20205842A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20006081A>T , CM000664.2:g.20006081A>T GRCh38
NC_000002.11:g.20205842A>T , CM000664.1:g.20205842A>T GRCh37
NC_000002.10:g.20069323A>T NCBI36
NG_008087.1:g.11614T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.453T>A MANE Select ENSP00000383894.3:p.Gly151=
ENST00000407540.7:c.453T>A ENSP00000383894.3:p.Gly151=
ENST00000421259.2:c.453T>A ENSP00000398753.2:p.Gly151=
NM_002381.4:c.453T>A NP_002372.1:p.Gly151=
NM_002381.5:c.453T>A MANE Select NP_002372.1:p.Gly151=
Search 100 bp 5'
Search 100 bp 3'