Canonical Allele Identifier: CA1907224420
Gene: MSMB HGNC NCBI

Linked Data

dbSNP Id: rs1840907635
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046622C>A , CM000672.2:g.46046622C>A GRCh38
NC_000010.10:g.51549200G>T , CM000672.1:g.51549200G>T GRCh37
NC_000010.9:g.51219206G>T NCBI36
NG_011551.1:g.4648G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-243G>T ENSP00000499419.1:n.-142-243G>T
Search 100 bp 5'
Search 100 bp 3'