Canonical Allele Identifier: CA2579835678
Gene: MSMB HGNC NCBI

Linked Data

gnomAD v4: 10-46046323-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.46046323G>T , CM000672.2:g.46046323G>T GRCh38
NC_000010.10:g.51549499C>A , CM000672.1:g.51549499C>A GRCh37
NC_000010.9:g.51219505C>A NCBI36
NG_011551.1:g.4947C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000663171.1:c.-86C>A ENSP00000499419.1:n.-86C>A
Search 100 bp 5'
Search 100 bp 3'