Canonical Allele Identifier: CA912970094
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs1554929506

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046600dup , CM000672.2:g.46046600dup GRCh38
NC_000010.10:g.51549222dup , CM000672.1:g.51549222dup GRCh37
NC_000010.9:g.51219228dup NCBI36
NG_011551.1:g.4670dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-221dup ENSP00000499419.1:n.-142-221dup