Canonical Allele Identifier: CA2579835977
Gene: MSMB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046417G>T , CM000672.2:g.46046417G>T GRCh38
NC_000010.10:g.51549405C>A , CM000672.1:g.51549405C>A GRCh37
NC_000010.9:g.51219411C>A NCBI36
NG_011551.1:g.4853C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000663171.1:c.-142-38C>A ENSP00000499419.1:n.-142-38C>A