Canonical Allele Identifier: CA1907224414
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs1590200857

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046614A>C , CM000672.2:g.46046614A>C GRCh38
NC_000010.10:g.51549208T>G , CM000672.1:g.51549208T>G GRCh37
NC_000010.9:g.51219214T>G NCBI36
NG_011551.1:g.4656T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-235T>G ENSP00000499419.1:n.-142-235T>G