Canonical Allele Identifier: CA593320520
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs1215712245

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046414T>A , CM000672.2:g.46046414T>A GRCh38
NC_000010.10:g.51549408A>T , CM000672.1:g.51549408A>T GRCh37
NC_000010.9:g.51219414A>T NCBI36
NG_011551.1:g.4856A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000663171.1:c.-142-35A>T ENSP00000499419.1:n.-142-35A>T