Canonical Allele Identifier: CA1907224383
Gene: MSMB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046599_46046600delinsAG , CM000672.2:g.46046599_46046600delinsAG GRCh38
NC_000010.10:g.51549222_51549223delinsCT , CM000672.1:g.51549222_51549223delinsCT GRCh37
NC_000010.9:g.51219228_51219229delinsCT NCBI36
NG_011551.1:g.4670_4671delinsCT

Transcript Alleles

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