Canonical Allele Identifier: CA992788634
Gene: MATK HGNC NCBI

Linked Data

dbSNP Id: rs2037602533
gnomAD v3: 19-3797123-T-C
gnomAD v4: 19-3797123-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3797123T>C , CM000681.2:g.3797123T>C GRCh38
NC_000019.9:g.3797121T>C , CM000681.1:g.3797121T>C GRCh37
NC_000019.8:g.3748121T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000395045.6:c.-58+4409A>G ENSP00000378485.1:n.-58+4409A>G
ENST00000590821.1:n.271+4409A>G
ENST00000590849.1:c.-52+4409A>G ENSP00000467992.1:n.-52+4409A>G
ENST00000590980.1:c.-58+4409A>G ENSP00000467472.1:n.-58+4409A>G
ENST00000592300.1:n.273-3722A>G
ENST00000592612.1:n.251-3725A>G
NM_002378.3:c.-58+4409A>G NP_002369.2:n.-58+4409A>G
XM_011528019.1:c.-58+4409A>G XP_011526321.1:n.-58+4409A>G
NM_002378.4:c.-58+4409A>G NP_002369.2:n.-58+4409A>G