Canonical Allele Identifier: CA2609005695
Gene: MSMB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046338_46046340del , CM000672.2:g.46046338_46046340del GRCh38
NC_000010.10:g.51549484_51549486del , CM000672.1:g.51549484_51549486del GRCh37
NC_000010.9:g.51219490_51219492del NCBI36
NG_011551.1:g.4932_4934del

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-101_-99del ENSP00000499419.1:n.-101_-99del