Canonical Allele Identifier: CA469555250
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs113588169
MyVariant Identifiers: chr10:g.51549186del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046636del , CM000672.2:g.46046636del GRCh38
NC_000010.10:g.51549188del , CM000672.1:g.51549188del GRCh37
NC_000010.9:g.51219194del NCBI36
NG_011551.1:g.4636del

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-255del ENSP00000499419.1:n.-142-255del