Canonical Allele Identifier: CA1907224422
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046623A= , CM000672.2:g.46046623A= GRCh38
NC_000010.10:g.51549199T= , CM000672.1:g.51549199T= GRCh37
NC_000010.9:g.51219205T= NCBI36
NG_011551.1:g.4647T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-244T= ENSP00000499419.1:n.-142-244T=