Canonical Allele Identifier: CA1907224352
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046576T= , CM000672.2:g.46046576T= GRCh38
NC_000010.10:g.51549246A= , CM000672.1:g.51549246A= GRCh37
NC_000010.9:g.51219252A= NCBI36
NG_011551.1:g.4694A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-197A= ENSP00000499419.1:n.-142-197A=