Canonical Allele Identifier: CA469555229
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs141211965

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046349G>A , CM000672.2:g.46046349G>A GRCh38
NC_000010.10:g.51549473C>T , CM000672.1:g.51549473C>T GRCh37
NC_000010.9:g.51219479C>T NCBI36
NG_011551.1:g.4921C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000663171.1:c.-112C>T ENSP00000499419.1:n.-112C>T