Canonical Allele Identifier: CA1543916
Gene: MATN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 1642858
ClinVar RCV Id: RCV002135687
dbSNP Id: rs371740669
ExAC: 2:20205563 G / A
gnomAD v2: 2-20205563-G-A
gnomAD v3: 2-20005802-G-A
gnomAD v4: 2-20005802-G-A
MyVariant Identifiers: chr2:g.20205563G>A (hg19) chr2:g.20005802G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20005802G>A , CM000664.2:g.20005802G>A GRCh38
NC_000002.11:g.20205563G>A , CM000664.1:g.20205563G>A GRCh37
NC_000002.10:g.20069044G>A NCBI36
NG_008087.1:g.11893C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.732C>T MANE Select ENSP00000383894.3:p.Tyr244=
ENST00000407540.7:c.732C>T ENSP00000383894.3:p.Tyr244=
ENST00000421259.2:c.732C>T ENSP00000398753.2:p.Tyr244=
NM_002381.4:c.732C>T NP_002372.1:p.Tyr244=
NM_002381.5:c.732C>T MANE Select NP_002372.1:p.Tyr244=
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