Canonical Allele Identifier: CA13105209
Gene: MOB3B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.27490969A>G , CM000671.2:g.27490969A>G GRCh38
NC_000009.11:g.27490967A>G , CM000671.1:g.27490967A>G GRCh37
NC_000009.10:g.27480967A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262244.6:c.-198-35221T>C MANE Select ENSP00000262244.5:n.-198-35221T>C
ENST00000262244.5:c.-198-35221T>C ENSP00000262244.5:n.-198-35221T>C
NM_024761.4:c.-198-35221T>C NP_079037.3:n.-198-35221T>C
NM_024761.5:c.-198-35221T>C MANE Select NP_079037.3:n.-198-35221T>C