Canonical Allele Identifier: CA2493007883
Gene: MATN3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20005898T= , CM000664.2:g.20005898T= GRCh38
NC_000002.11:g.20205659T= , CM000664.1:g.20205659T= GRCh37
NC_000002.10:g.20069140T= NCBI36
NG_008087.1:g.11797A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.636A= MANE Select ENSP00000383894.3:p.Ala212=
ENST00000407540.7:c.636A= ENSP00000383894.3:p.Ala212=
ENST00000421259.2:c.636A= ENSP00000398753.2:p.Ala212=
NM_002381.4:c.636A= NP_002372.1:p.Ala212=
NM_002381.5:c.636A= MANE Select NP_002372.1:p.Ala212=
Search 100 bp 5'
Search 100 bp 3'