Canonical Allele Identifier: CA2579835786
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046357A>T , CM000672.2:g.46046357A>T GRCh38
NC_000010.10:g.51549465T>A , CM000672.1:g.51549465T>A GRCh37
NC_000010.9:g.51219471T>A NCBI36
NG_011551.1:g.4913T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-120T>A ENSP00000499419.1:n.-120T>A