Canonical Allele Identifier: CA2579834699
Gene: MSMB HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046541A>T , CM000672.2:g.46046541A>T GRCh38
NC_000010.10:g.51549281T>A , CM000672.1:g.51549281T>A GRCh37
NC_000010.9:g.51219287T>A NCBI36
NG_011551.1:g.4729T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-162T>A ENSP00000499419.1:n.-142-162T>A
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