Canonical Allele Identifier: CA912970095
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs1554929507

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046600_46046601insA , CM000672.2:g.46046600_46046601insA GRCh38
NC_000010.10:g.51549221_51549222insT , CM000672.1:g.51549221_51549222insT GRCh37
NC_000010.9:g.51219227_51219228insT NCBI36
NG_011551.1:g.4669_4670insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-222_-142-221insT ENSP00000499419.1:n.-142-222_-142-221insT