Canonical Allele Identifier: CA2579834766
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046563T>A , CM000672.2:g.46046563T>A GRCh38
NC_000010.10:g.51549259A>T , CM000672.1:g.51549259A>T GRCh37
NC_000010.9:g.51219265A>T NCBI36
NG_011551.1:g.4707A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-184A>T ENSP00000499419.1:n.-142-184A>T