Canonical Allele Identifier: CA2493007969
Gene: MATN3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20006074T= , CM000664.2:g.20006074T= GRCh38
NC_000002.11:g.20205835T= , CM000664.1:g.20205835T= GRCh37
NC_000002.10:g.20069316T= NCBI36
NG_008087.1:g.11621A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.460A= MANE Select ENSP00000383894.3:p.Thr154=
ENST00000407540.7:c.460A= ENSP00000383894.3:p.Thr154=
ENST00000421259.2:c.460A= ENSP00000398753.2:p.Thr154=
NM_002381.4:c.460A= NP_002372.1:p.Thr154=
NM_002381.5:c.460A= MANE Select NP_002372.1:p.Thr154=
Search 100 bp 5'
Search 100 bp 3'