Canonical Allele Identifier: CA425340889
Gene: MATN3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.20205569A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20005808A>T , CM000664.2:g.20005808A>T GRCh38
NC_000002.11:g.20205569A>T , CM000664.1:g.20205569A>T GRCh37
NC_000002.10:g.20069050A>T NCBI36
NG_008087.1:g.11887T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.726T>A MANE Select ENSP00000383894.3:p.Val242=
ENST00000407540.7:c.726T>A ENSP00000383894.3:p.Val242=
ENST00000421259.2:c.726T>A ENSP00000398753.2:p.Val242=
NM_002381.4:c.726T>A NP_002372.1:p.Val242=
NM_002381.5:c.726T>A MANE Select NP_002372.1:p.Val242=
Search 100 bp 5'
Search 100 bp 3'