Canonical Allele Identifier: CA2579834815
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046578C>G , CM000672.2:g.46046578C>G GRCh38
NC_000010.10:g.51549244G>C , CM000672.1:g.51549244G>C GRCh37
NC_000010.9:g.51219250G>C NCBI36
NG_011551.1:g.4692G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-199G>C ENSP00000499419.1:n.-142-199G>C