Canonical Allele Identifier: CA665634286
Gene: MSMB HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.46046600_46046601insT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046600_46046601insT , CM000672.2:g.46046600_46046601insT GRCh38
NC_000010.10:g.51549221_51549222insA , CM000672.1:g.51549221_51549222insA GRCh37
NC_000010.9:g.51219227_51219228insA NCBI36
NG_011551.1:g.4669_4670insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-142-222_-142-221insA ENSP00000499419.1:n.-142-222_-142-221insA
Search 100 bp 5'
Search 100 bp 3'