Canonical Allele Identifier: CA2579834751
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046557A>C , CM000672.2:g.46046557A>C GRCh38
NC_000010.10:g.51549265T>G , CM000672.1:g.51549265T>G GRCh37
NC_000010.9:g.51219271T>G NCBI36
NG_011551.1:g.4713T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-178T>G ENSP00000499419.1:n.-142-178T>G