Canonical Allele Identifier: CA2658010800
Gene: MATN3 HGNC NCBI

Linked Data

gnomAD v4: 2-20005597-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.20005597T>C , CM000664.2:g.20005597T>C GRCh38
NC_000002.11:g.20205358T>C , CM000664.1:g.20205358T>C GRCh37
NC_000002.10:g.20068839T>C NCBI36
NG_008087.1:g.12098A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000407540.8:c.790+147A>G MANE Select ENSP00000383894.3:n.790+147A>G
ENST00000407540.7:c.790+147A>G ENSP00000383894.3:n.790+147A>G
ENST00000421259.2:c.790+147A>G ENSP00000398753.2:n.790+147A>G
NM_002381.4:c.790+147A>G NP_002372.1:n.790+147A>G
NM_002381.5:c.790+147A>G MANE Select NP_002372.1:n.790+147A>G