Canonical Allele Identifier: CA918665654
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs1554929498

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046599dup , CM000672.2:g.46046599dup GRCh38
NC_000010.10:g.51549223dup , CM000672.1:g.51549223dup GRCh37
NC_000010.9:g.51219229dup NCBI36
NG_011551.1:g.4671dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-220dup ENSP00000499419.1:n.-142-220dup