Canonical Allele Identifier: CA2579835982
Gene: MSMB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046418T>C , CM000672.2:g.46046418T>C GRCh38
NC_000010.10:g.51549404A>G , CM000672.1:g.51549404A>G GRCh37
NC_000010.9:g.51219410A>G NCBI36
NG_011551.1:g.4852A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000663171.1:c.-142-39A>G ENSP00000499419.1:n.-142-39A>G