Canonical Allele Identifier: CA2579835991
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046421T>G , CM000672.2:g.46046421T>G GRCh38
NC_000010.10:g.51549401A>C , CM000672.1:g.51549401A>C GRCh37
NC_000010.9:g.51219407A>C NCBI36
NG_011551.1:g.4849A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-42A>C ENSP00000499419.1:n.-142-42A>C