Canonical Allele Identifier: CA1907224219
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046431A= , CM000672.2:g.46046431A= GRCh38
NC_000010.10:g.51549391T= , CM000672.1:g.51549391T= GRCh37
NC_000010.9:g.51219397T= NCBI36
NG_011551.1:g.4839T=

Transcript Alleles

HGVS Amino-acid change
ENST00000663171.1:c.-142-52T= ENSP00000499419.1:n.-142-52T=