Canonical Allele Identifier: CA2579835946
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046408G>A , CM000672.2:g.46046408G>A GRCh38
NC_000010.10:g.51549414C>T , CM000672.1:g.51549414C>T GRCh37
NC_000010.9:g.51219420C>T NCBI36
NG_011551.1:g.4862C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000663171.1:c.-142-29C>T ENSP00000499419.1:n.-142-29C>T