Canonical Allele Identifier: CA2698865586
Gene: MATN3 HGNC NCBI
WDR35-DT HGNC NCBI

Linked Data

dbSNP Id: rs2103480146
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.19998112C>T , CM000664.2:g.19998112C>T GRCh38
NC_000002.11:g.20197873C>T , CM000664.1:g.20197873C>T GRCh37
NC_000002.10:g.20061354C>T NCBI36
NG_008087.1:g.19583G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.1169-853G>A (MATN3) MANE Select ENSP00000383894.3:n.1169-853G>A
ENST00000407540.7:c.1169-853G>A (MATN3) ENSP00000383894.3:n.1169-853G>A
ENST00000421259.2:c.1043-853G>A (MATN3) ENSP00000398753.2:n.1043-853G>A
NM_002381.4:c.1169-853G>A (MATN3) NP_002372.1:n.1169-853G>A
NR_110235.1:n.292-1094C>T (WDR35-DT)
NM_002381.5:c.1169-853G>A (MATN3) MANE Select NP_002372.1:n.1169-853G>A
Search 100 bp 5'
Search 100 bp 3'