Canonical Allele Identifier: CA1907224419
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046622C= , CM000672.2:g.46046622C= GRCh38
NC_000010.10:g.51549200G= , CM000672.1:g.51549200G= GRCh37
NC_000010.9:g.51219206G= NCBI36
NG_011551.1:g.4648G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-243G= ENSP00000499419.1:n.-142-243G=