Canonical Allele Identifier: CA2835580605
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046600_46046601insTG , CM000672.2:g.46046600_46046601insTG GRCh38
NC_000010.10:g.51549222_51549223insAC , CM000672.1:g.51549222_51549223insAC GRCh37
NC_000010.9:g.51219228_51219229insAC NCBI36
NG_011551.1:g.4670_4671insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-221_-142-220insAC ENSP00000499419.1:n.-142-221_-142-220insAC