Canonical Allele Identifier: CA345951089
Gene: MATN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1675210
ClinVar RCV Id: RCV002210946
dbSNP Id: rs2103484073
MyVariant Identifiers: chr2:g.20205858A>C (hg19) chr2:g.20006097A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20006097A>C , CM000664.2:g.20006097A>C GRCh38
NC_000002.11:g.20205858A>C , CM000664.1:g.20205858A>C GRCh37
NC_000002.10:g.20069339A>C NCBI36
NG_008087.1:g.11598T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.437T>G MANE Select ENSP00000383894.3:p.Leu146Arg
ENST00000407540.7:c.437T>G ENSP00000383894.3:p.Leu146Arg
ENST00000421259.2:c.437T>G ENSP00000398753.2:p.Leu146Arg
NM_002381.4:c.437T>G NP_002372.1:p.Leu146Arg
NM_002381.5:c.437T>G MANE Select NP_002372.1:p.Leu146Arg
Search 100 bp 5'
Search 100 bp 3'