Canonical Allele Identifier: CA2579835681
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046324A>T , CM000672.2:g.46046324A>T GRCh38
NC_000010.10:g.51549498T>A , CM000672.1:g.51549498T>A GRCh37
NC_000010.9:g.51219504T>A NCBI36
NG_011551.1:g.4946T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-87T>A ENSP00000499419.1:n.-87T>A