Canonical Allele Identifier: CA2579834916
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046614A>G , CM000672.2:g.46046614A>G GRCh38
NC_000010.10:g.51549208T>C , CM000672.1:g.51549208T>C GRCh37
NC_000010.9:g.51219214T>C NCBI36
NG_011551.1:g.4656T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-235T>C ENSP00000499419.1:n.-142-235T>C