Canonical Allele Identifier: CA1907224417
Gene: MSMB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046622_46046623delinsCA , CM000672.2:g.46046622_46046623delinsCA GRCh38
NC_000010.10:g.51549199_51549200delinsTG , CM000672.1:g.51549199_51549200delinsTG GRCh37
NC_000010.9:g.51219205_51219206delinsTG NCBI36
NG_011551.1:g.4647_4648delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-244_-142-243delinsTG ENSP00000499419.1:n.-142-244_-142-243delinsTG
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