Canonical Allele Identifier: CA2579834761
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046559C>T , CM000672.2:g.46046559C>T GRCh38
NC_000010.10:g.51549263G>A , CM000672.1:g.51549263G>A GRCh37
NC_000010.9:g.51219269G>A NCBI36
NG_011551.1:g.4711G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-180G>A ENSP00000499419.1:n.-142-180G>A