Canonical Allele Identifier: CA2579835832
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046371G>C , CM000672.2:g.46046371G>C GRCh38
NC_000010.10:g.51549451C>G , CM000672.1:g.51549451C>G GRCh37
NC_000010.9:g.51219457C>G NCBI36
NG_011551.1:g.4899C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-134C>G ENSP00000499419.1:n.-134C>G