Canonical Allele Identifier: CA927917150
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs1840907891
gnomAD v3: 10-46046622-CA-C
gnomAD v4: 10-46046622-CA-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046623del , CM000672.2:g.46046623del GRCh38
NC_000010.10:g.51549199del , CM000672.1:g.51549199del GRCh37
NC_000010.9:g.51219205del NCBI36
NG_011551.1:g.4647del

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-244del ENSP00000499419.1:n.-142-244del
Search 100 bp 5'
Search 100 bp 3'