Canonical Allele Identifier: CA43403389
Gene: MATN3 HGNC NCBI

Linked Data

dbSNP Id: rs999084190
gnomAD v3: 2-20005671-A-T
gnomAD v4: 2-20005671-A-T
MyVariant Identifiers: chr2:g.20205432A>T (hg19) chr2:g.20005671A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20005671A>T , CM000664.2:g.20005671A>T GRCh38
NC_000002.11:g.20205432A>T , CM000664.1:g.20205432A>T GRCh37
NC_000002.10:g.20068913A>T NCBI36
NG_008087.1:g.12024T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.790+73T>A MANE Select ENSP00000383894.3:n.790+73T>A
ENST00000407540.7:c.790+73T>A ENSP00000383894.3:n.790+73T>A
ENST00000421259.2:c.790+73T>A ENSP00000398753.2:n.790+73T>A
NM_002381.4:c.790+73T>A NP_002372.1:n.790+73T>A
NM_002381.5:c.790+73T>A MANE Select NP_002372.1:n.790+73T>A
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