Canonical Allele Identifier: CA2609005688
Gene: MSMB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046281_46046427del , CM000672.2:g.46046281_46046427del GRCh38
NC_000010.10:g.51549396_51549542del , CM000672.1:g.51549396_51549542del GRCh37
NC_000010.9:g.51219402_51219548del NCBI36
NG_011551.1:g.4844_4990del

Transcript Alleles

HGVS Amino-acid change
ENST00000663171.1:c.-142-47_-43del