Canonical Allele Identifier: CA881962530
Gene: MATK HGNC NCBI

Linked Data

dbSNP Id: rs1457441595

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3797034G>A , CM000681.2:g.3797034G>A GRCh38
NC_000019.9:g.3797032G>A , CM000681.1:g.3797032G>A GRCh37
NC_000019.8:g.3748032G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000395045.6:c.-58+4498C>T ENSP00000378485.1:n.-58+4498C>T
ENST00000590821.1:n.271+4498C>T
ENST00000590849.1:c.-52+4498C>T ENSP00000467992.1:n.-52+4498C>T
ENST00000590980.1:c.-58+4498C>T ENSP00000467472.1:n.-58+4498C>T
ENST00000592300.1:n.273-3633C>T
ENST00000592612.1:n.251-3636C>T
NM_002378.3:c.-58+4498C>T NP_002369.2:n.-58+4498C>T
XM_011528019.1:c.-58+4498C>T XP_011526321.1:n.-58+4498C>T
NM_002378.4:c.-58+4498C>T NP_002369.2:n.-58+4498C>T