Canonical Allele Identifier: CA2579835837
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046373G= , CM000672.2:g.46046373G= GRCh38
NC_000010.10:g.51549449C= , CM000672.1:g.51549449C= GRCh37
NC_000010.9:g.51219455C= NCBI36
NG_011551.1:g.4897C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-136C= ENSP00000499419.1:n.-136C=